Canonical Allele Identifier: CA2184934365

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335803A= , CM000677.2:g.68335803A=	GRCh38
NC_000015.9:g.68628141A= , CM000677.1:g.68628141A=	GRCh37
NC_000015.8:g.66415195A=	NCBI36
NG_046911.1:g.101358T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1319T= MANE Select	ENSP00000327290.7:p.Val440=
ENST00000315757.8:c.1319T=	ENSP00000327290.7:p.Val440=
ENST00000423218.6:c.1319T=	ENSP00000403392.2:p.Val440=
ENST00000566429.1:n.208T=
ENST00000569346.5:n.298T=
NM_001004439.1:c.1319T=	NP_001004439.1:p.Val440=
XM_005254228.2:c.1013T=	XP_005254285.1:p.Val338=
XM_011521363.1:c.1112T=	XP_011519665.1:p.Val371=
XM_005254228.3:c.1013T=	XP_005254285.1:p.Val338=
XM_011521363.2:c.1112T=	XP_011519665.1:p.Val371=
NM_001004439.2:c.1319T= MANE Select	NP_001004439.1:p.Val440=