Canonical Allele Identifier: CA431535021

Gene: TRIP12

Linked Data

• MyVariant Identifiers: chr2:g.230652287G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.229787571G>A , CM000664.2:g.229787571G>A	GRCh38
NC_000002.11:g.230652287G>A , CM000664.1:g.230652287G>A	GRCh37
NC_000002.10:g.230360531G>A	NCBI36
NG_053017.1:g.140664C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430954.6:c.4752C>T	ENSP00000389827.2:p.Thr1584=
ENST00000453485.2:c.4761C>T	ENSP00000400967.2:p.Thr1587=
ENST00000704577.1:c.4929C>T	ENSP00000515952.1:p.Thr1643=
ENST00000704578.1:c.4788C>T	ENSP00000515953.1:p.Thr1596=
ENST00000704579.1:c.*3093C>T	ENSP00000515954.1:n.*3093C>T
ENST00000704580.1:c.4803C>T	ENSP00000515955.1:p.Thr1601=
ENST00000704581.1:c.4917C>T	ENSP00000515956.1:p.Thr1639=
ENST00000704582.1:c.583C>T
ENST00000704583.1:c.*2413C>T	ENSP00000515958.1:n.*2413C>T
ENST00000704584.1:c.4652C>T
ENST00000704585.1:c.4707C>T	ENSP00000515960.1:p.Thr1569=
ENST00000675423.1:c.4929C>T	ENSP00000502768.1:p.Thr1643=
ENST00000675453.1:c.4932C>T	ENSP00000502271.1:p.Thr1644=
ENST00000675903.1:c.4929C>T MANE Select	ENSP00000502713.1:p.Thr1643=
ENST00000283943.9:c.4704C>T	ENSP00000283943.4:p.Thr1568=
ENST00000389044.8:c.4848C>T	ENSP00000373696.4:p.Thr1616=
ENST00000389045.7:c.3894C>T	ENSP00000373697.3:p.Thr1298=
NM_001284214.1:c.4848C>T	NP_001271143.1:p.Thr1616=
NM_001284215.1:c.4803C>T	NP_001271144.1:p.Thr1601=
NM_001284216.1:c.3894C>T	NP_001271145.1:p.Thr1298=
NM_004238.2:c.4704C>T	NP_004229.1:p.Thr1568=
XM_005246954.3:c.4932C>T	XP_005247011.1:p.Thr1644=
XM_005246955.3:c.4932C>T	XP_005247012.1:p.Thr1644=
XM_005246956.3:c.4929C>T	XP_005247013.1:p.Thr1643=
XM_005246957.3:c.4917C>T	XP_005247014.1:p.Thr1639=
XM_005246958.3:c.4851C>T	XP_005247015.1:p.Thr1617=
XM_005246960.3:c.4845C>T	XP_005247017.1:p.Thr1615=
XM_005246961.2:c.4806C>T	XP_005247018.1:p.Thr1602=
XM_005246962.3:c.4803C>T	XP_005247019.1:p.Thr1601=
XM_005246963.3:c.4932C>T	XP_005247020.1:p.Thr1644=
XM_006712852.2:c.4806C>T	XP_006712915.1:p.Thr1602=
XM_006712853.2:c.4722C>T	XP_006712916.1:p.Thr1574=
XM_011512180.1:c.4932C>T	XP_011510482.1:p.Thr1644=
XM_011512181.1:c.4932C>T	XP_011510483.1:p.Thr1644=
XM_011512182.1:c.4932C>T	XP_011510484.1:p.Thr1644=
XM_011512183.1:c.4806C>T	XP_011510485.1:p.Thr1602=
XM_011512184.1:c.4932C>T	XP_011510486.1:p.Thr1644=
NM_001284215.2:c.4803C>T	NP_001271144.1:p.Thr1601=
NM_001348315.1:c.4848C>T	NP_001335244.1:p.Thr1616=
NM_001348316.1:c.4803C>T	NP_001335245.1:p.Thr1601=
NM_001348317.1:c.4788C>T	NP_001335246.1:p.Thr1596=
NM_001348318.1:c.4788C>T	NP_001335247.1:p.Thr1596=
NM_001348319.1:c.4914C>T	NP_001335248.1:p.Thr1638=
NM_001348320.1:c.4914C>T	NP_001335249.1:p.Thr1638=
NM_001348321.1:c.4917C>T	NP_001335250.1:p.Thr1639=
NM_001348322.1:c.4929C>T	NP_001335251.1:p.Thr1643=
NM_001348323.1:c.4929C>T	NP_001335252.1:p.Thr1643=
NM_001348324.1:c.4929C>T	NP_001335253.1:p.Thr1643=
NM_001348325.1:c.4929C>T	NP_001335254.1:p.Thr1643=
NM_001348326.1:c.4929C>T	NP_001335255.1:p.Thr1643=
NM_001348327.1:c.4929C>T	NP_001335256.1:p.Thr1643=
NM_001348328.1:c.4932C>T	NP_001335257.1:p.Thr1644=
NM_001348329.1:c.4932C>T	NP_001335258.1:p.Thr1644=
NM_001348330.1:c.4932C>T	NP_001335259.1:p.Thr1644=
NM_001348331.1:c.4707C>T	NP_001335260.1:p.Thr1569=
NM_001348332.1:c.4827C>T	NP_001335261.1:p.Thr1609=
NM_001348333.1:c.4851C>T	NP_001335262.1:p.Thr1617=
XM_005246961.4:c.4806C>T	XP_005247018.1:p.Thr1602=
XM_017005283.2:c.4833C>T	XP_016860772.1:p.Thr1611=
XM_017005289.2:c.4764C>T	XP_016860778.1:p.Thr1588=
XM_017005290.2:c.4761C>T	XP_016860779.1:p.Thr1587=
XM_024453223.1:c.5004C>T	XP_024308991.1:p.Thr1668=
XM_024453224.1:c.5004C>T	XP_024308992.1:p.Thr1668=
XM_024453225.1:c.5004C>T	XP_024308993.1:p.Thr1668=
XM_024453226.1:c.5004C>T	XP_024308994.1:p.Thr1668=
XM_024453227.1:c.5004C>T	XP_024308995.1:p.Thr1668=
XM_024453228.1:c.5004C>T	XP_024308996.1:p.Thr1668=
XM_024453229.1:c.5001C>T	XP_024308997.1:p.Thr1667=
XM_024453230.1:c.5001C>T	XP_024308998.1:p.Thr1667=
XM_024453231.1:c.4923C>T	XP_024308999.1:p.Thr1641=
XM_024453232.1:c.4920C>T	XP_024309000.1:p.Thr1640=
XM_024453233.1:c.4917C>T	XP_024309001.1:p.Thr1639=
XM_024453234.1:c.4917C>T	XP_024309002.1:p.Thr1639=
XM_024453235.1:c.4917C>T	XP_024309003.1:p.Thr1639=
XM_024453236.1:c.4878C>T	XP_024309004.1:p.Thr1626=
XM_024453237.1:c.4878C>T	XP_024309005.1:p.Thr1626=
XM_024453238.1:c.4878C>T	XP_024309006.1:p.Thr1626=
XM_024453239.1:c.4878C>T	XP_024309007.1:p.Thr1626=
XM_024453240.1:c.4878C>T	XP_024309008.1:p.Thr1626=
XM_024453241.1:c.4875C>T	XP_024309009.1:p.Thr1625=
XM_024453242.1:c.4791C>T	XP_024309010.1:p.Thr1597=
XM_024453243.1:c.4722C>T	XP_024309011.1:p.Thr1574=
NM_001284214.2:c.4848C>T	NP_001271143.1:p.Thr1616=
NM_001284216.2:c.3894C>T	NP_001271145.1:p.Thr1298=
NM_001348315.2:c.4848C>T	NP_001335244.1:p.Thr1616=
NM_001348316.2:c.4803C>T	NP_001335245.1:p.Thr1601=
NM_001348318.2:c.4788C>T	NP_001335247.1:p.Thr1596=
NM_001348320.2:c.4914C>T	NP_001335249.1:p.Thr1638=
NM_001348323.2:c.4929C>T	NP_001335252.1:p.Thr1643=
NM_001348324.2:c.4929C>T	NP_001335253.1:p.Thr1643=
NM_001348325.2:c.4929C>T	NP_001335254.1:p.Thr1643=
NM_001348326.2:c.4929C>T	NP_001335255.1:p.Thr1643=
NM_001348327.2:c.4929C>T	NP_001335256.1:p.Thr1643=
NM_001348329.2:c.4932C>T	NP_001335258.1:p.Thr1644=
NM_001348330.2:c.4932C>T	NP_001335259.1:p.Thr1644=
NM_004238.3:c.4704C>T	NP_004229.1:p.Thr1568=
NM_001348323.3:c.4929C>T MANE Select	NP_001335252.1:p.Thr1643=