Canonical Allele Identifier: CA427568950

Gene: INPP4A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98520084C>T , CM000664.2:g.98520084C>T	GRCh38
NC_000002.11:g.99136547C>T , CM000664.1:g.99136547C>T	GRCh37
NC_000002.10:g.98502979C>T	NCBI36
NG_029890.1:g.80227C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001134225.2:c.36C>T MANE Select	NP_001127697.1:p.Ala12=
ENST00000409851.8:c.36C>T MANE Select	ENSP00000386777.4:p.Ala12=
NM_001134224.1:c.36C>T	NP_001127696.1:p.Ala12=
NM_001134224.2:c.36C>T	NP_001127696.1:p.Ala12=
NM_001134225.1:c.36C>T	NP_001127697.1:p.Ala12=
NM_001351424.1:c.36C>T	NP_001338353.1:p.Ala12=
NM_001351425.1:c.36C>T	NP_001338354.1:p.Ala12=
NM_001351425.2:c.36C>T	NP_001338354.1:p.Ala12=
NM_001351426.1:c.36C>T	NP_001338355.1:p.Ala12=
NM_001351426.2:c.36C>T	NP_001338355.1:p.Ala12=
NM_001351427.1:c.36C>T	NP_001338356.1:p.Ala12=
NM_001351427.2:c.36C>T	NP_001338356.1:p.Ala12=
NM_001351428.1:c.36C>T	NP_001338357.1:p.Ala12=
NM_001351428.2:c.36C>T	NP_001338357.1:p.Ala12=
NM_001351429.1:c.36C>T	NP_001338358.1:p.Ala12=
NM_001351429.2:c.36C>T	NP_001338358.1:p.Ala12=
NM_001566.2:c.36C>T	NP_001557.1:p.Ala12=
NM_004027.2:c.36C>T	NP_004018.1:p.Ala12=
NM_004027.3:c.36C>T	NP_004018.1:p.Ala12=
ENST00000074304.9:c.36C>T	ENSP00000074304.5:p.Ala12=
ENST00000409016.8:c.36C>T	ENSP00000386704.3:p.Ala12=
ENST00000409463.5:c.36C>T	ENSP00000386329.1:p.Ala12=
ENST00000409540.7:c.36C>T	ENSP00000387294.3:p.Ala12=
ENST00000409851.7:c.36C>T	ENSP00000386777.3:p.Ala12=
ENST00000463367.1:n.855C>T
ENST00000523221.1:c.36C>T	ENSP00000427722.1:p.Ala12=
ENST00000706935.1:c.36C>T	ENSP00000516656.1:p.Ala12=
XM_006712499.2:c.36C>T	XP_006712562.1:p.Ala12=
XM_006712499.3:c.36C>T	XP_006712562.1:p.Ala12=
XM_006712500.2:c.36C>T	XP_006712563.1:p.Ala12=
XM_006712500.3:c.36C>T	XP_006712563.1:p.Ala12=
XM_006712501.2:c.36C>T	XP_006712564.1:p.Ala12=
XM_006712501.3:c.36C>T	XP_006712564.1:p.Ala12=
XM_006712502.2:c.36C>T	XP_006712565.1:p.Ala12=
XM_006712502.3:c.36C>T	XP_006712565.1:p.Ala12=
XM_006712503.2:c.36C>T	XP_006712566.1:p.Ala12=
XM_006712503.3:c.36C>T	XP_006712566.1:p.Ala12=
XM_006712504.2:c.36C>T	XP_006712567.1:p.Ala12=
XM_006712504.3:c.36C>T	XP_006712567.1:p.Ala12=
XM_006712505.2:c.36C>T	XP_006712568.1:p.Ala12=
XM_006712505.3:c.36C>T	XP_006712568.1:p.Ala12=
XM_006712506.2:c.36C>T	XP_006712569.1:p.Ala12=
XM_006712506.3:c.36C>T	XP_006712569.1:p.Ala12=
XM_006712507.2:c.36C>T	XP_006712570.1:p.Ala12=
XM_006712508.2:c.36C>T	XP_006712571.1:p.Ala12=
XM_006712508.3:c.36C>T	XP_006712571.1:p.Ala12=
XM_011511122.1:c.36C>T	XP_011509424.1:p.Ala12=
XM_011511122.2:c.36C>T	XP_011509424.1:p.Ala12=
XM_011511123.1:c.36C>T	XP_011509425.1:p.Ala12=
XM_011511123.2:c.36C>T	XP_011509425.1:p.Ala12=
XM_011511124.1:c.36C>T	XP_011509426.1:p.Ala12=
XM_011511124.2:c.36C>T	XP_011509426.1:p.Ala12=
XM_017003994.1:c.36C>T	XP_016859483.1:p.Ala12=
XM_017003995.1:c.36C>T	XP_016859484.1:p.Ala12=
XM_017003996.1:c.36C>T	XP_016859485.1:p.Ala12=
XM_017004000.1:c.36C>T	XP_016859489.1:p.Ala12=
XM_017004001.1:c.36C>T	XP_016859490.1:p.Ala12=
XM_017004003.1:c.36C>T	XP_016859492.1:p.Ala12=
XM_024452876.1:c.36C>T	XP_024308644.1:p.Ala12=
XR_001738737.1:n.424C>T
XR_001738738.1:n.424C>T
XR_922915.1:n.429C>T
XR_922915.2:n.424C>T
XR_922916.1:n.429C>T
XR_922916.2:n.424C>T