Canonical Allele Identifier: CA489892882

Gene: TTBK2

Linked Data

• MyVariant Identifiers: chr15:g.43069255T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42777057T>C , CM000677.2:g.42777057T>C	GRCh38
NC_000015.9:g.43069255T>C , CM000677.1:g.43069255T>C	GRCh37
NC_000015.8:g.40856547T>C	NCBI36
NG_012664.1:g.148753A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000267890.11:c.1383A>G MANE Select	ENSP00000267890.6:p.Pro461=
ENST00000267890.10:c.1383A>G	ENSP00000267890.6:p.Pro461=
ENST00000567274.5:c.1278A>G	ENSP00000457489.1:p.Pro426=
ENST00000567840.5:c.1383A>G	ENSP00000455734.1:p.Pro461=
ENST00000622375.4:c.2598A>G	ENSP00000479984.1:p.Pro866=
NM_173500.3:c.1383A>G	NP_775771.3:p.Pro461=
XM_005254171.3:c.1401A>G	XP_005254228.1:p.Pro467=
XM_005254173.3:c.1176A>G	XP_005254230.1:p.Pro392=
XM_006720402.2:c.1368A>G	XP_006720465.1:p.Pro456=
XM_006720403.2:c.1176A>G	XP_006720466.1:p.Pro392=
XM_011521267.1:c.1176A>G	XP_011519569.1:p.Pro392=
XM_011521268.1:c.1116A>G	XP_011519570.1:p.Pro372=
XM_011521269.1:c.1104A>G	XP_011519571.1:p.Pro368=
XM_005254171.5:c.1401A>G	XP_005254228.1:p.Pro467=
XM_005254173.5:c.1176A>G	XP_005254230.1:p.Pro392=
XM_006720402.4:c.1368A>G	XP_006720465.1:p.Pro456=
XM_006720403.4:c.1176A>G	XP_006720466.1:p.Pro392=
XM_017021950.2:c.1104A>G	XP_016877439.1:p.Pro368=
XM_024449849.1:c.1383A>G	XP_024305617.1:p.Pro461=
XM_024449850.1:c.1383A>G	XP_024305618.1:p.Pro461=
XM_024449851.1:c.1176A>G	XP_024305619.1:p.Pro392=
NM_173500.4:c.1383A>G MANE Select	NP_775771.3:p.Pro461=