Canonical Allele Identifier: CA2184934302

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335676C= , CM000677.2:g.68335676C=	GRCh38
NC_000015.9:g.68628014C= , CM000677.1:g.68628014C=	GRCh37
NC_000015.8:g.66415068C=	NCBI36
NG_046911.1:g.101485G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+21G= MANE Select	ENSP00000327290.7:n.1425+21G=
ENST00000315757.8:c.1425+21G=	ENSP00000327290.7:n.1425+21G=
ENST00000423218.6:c.1425+21G=	ENSP00000403392.2:n.1425+21G=
ENST00000566429.1:n.314+21G=
ENST00000569346.5:n.404+21G=
NM_001004439.1:c.1425+21G=	NP_001004439.1:n.1425+21G=
XM_005254228.2:c.1119+21G=	XP_005254285.1:n.1119+21G=
XM_011521363.1:c.1218+21G=	XP_011519665.1:n.1218+21G=
XM_005254228.3:c.1119+21G=	XP_005254285.1:n.1119+21G=
XM_011521363.2:c.1218+21G=	XP_011519665.1:n.1218+21G=
NM_001004439.2:c.1425+21G= MANE Select	NP_001004439.1:n.1425+21G=