Canonical Allele Identifier: CA1056536

Gene: ITGA10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.145896844C>T , CM000663.2:g.145896844C>T	GRCh38
NC_000001.10:g.145538232G>A , CM000663.1:g.145538232G>A	GRCh37
NC_000001.9:g.144249589G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369304.8:c.2759G>A MANE Select	ENSP00000358310.3:p.Arg920Lys
ENST00000369304.7:c.2759G>A	ENSP00000358310.3:p.Arg920Lys
ENST00000539363.2:c.2330G>A	ENSP00000439894.1:p.Arg777Lys
NM_001303040.1:c.2366G>A	NP_001289969.1:p.Arg789Lys
NM_001303041.1:c.2330G>A	NP_001289970.1:p.Arg777Lys
NM_003637.4:c.2759G>A	NP_003628.2:p.Arg920Lys
XM_005277436.2:c.2573G>A	XP_005277493.1:p.Arg858Lys
XM_011510079.1:c.2756G>A	XP_011508381.1:p.Arg919Lys
XM_011510080.1:c.2657G>A	XP_011508382.1:p.Arg886Lys
XM_011510081.1:c.2759G>A	XP_011508383.1:p.Arg920Lys
XM_011510082.1:c.2759G>A	XP_011508384.1:p.Arg920Lys
XM_011510083.1:c.2264G>A	XP_011508385.1:p.Arg755Lys
XM_011510084.1:c.1232G>A	XP_011508386.1:p.Arg411Lys
XR_921987.1:n.3153G>A
XR_921988.1:n.3153G>A
XR_921989.1:n.3154G>A
XM_005277436.3:c.2573G>A	XP_005277493.1:p.Arg858Lys
XM_011510083.2:c.2264G>A	XP_011508385.1:p.Arg755Lys
XM_017002622.1:c.2801G>A	XP_016858111.1:p.Arg934Lys
XM_017002623.1:c.2798G>A	XP_016858112.1:p.Arg933Lys
XM_017002624.1:c.2801G>A	XP_016858113.1:p.Arg934Lys
XM_017002625.1:c.2801G>A	XP_016858114.1:p.Arg934Lys
XM_017002626.1:c.2558G>A	XP_016858115.1:p.Arg853Lys
XM_017002628.1:c.1646G>A	XP_016858117.1:p.Arg549Lys
XR_001737501.1:n.2891G>A
XR_001737502.1:n.2891G>A
XR_001737503.1:n.2891G>A
XR_001737504.1:n.2910G>A
NM_003637.5:c.2759G>A MANE Select	NP_003628.2:p.Arg920Lys
NM_001303040.2:c.2366G>A	NP_001289969.1:p.Arg789Lys
NM_001303041.2:c.2330G>A	NP_001289970.1:p.Arg777Lys