Canonical Allele Identifier: CA2184934383

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335844C= , CM000677.2:g.68335844C=	GRCh38
NC_000015.9:g.68628182C= , CM000677.1:g.68628182C=	GRCh37
NC_000015.8:g.66415236C=	NCBI36
NG_046911.1:g.101317G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1278G= MANE Select	ENSP00000327290.7:p.Gly426=
ENST00000315757.8:c.1278G=	ENSP00000327290.7:p.Gly426=
ENST00000423218.6:c.1278G=	ENSP00000403392.2:p.Gly426=
ENST00000566429.1:n.197-30G=
ENST00000569346.5:n.257G=
NM_001004439.1:c.1278G=	NP_001004439.1:p.Gly426=
XM_005254228.2:c.972G=	XP_005254285.1:p.Gly324=
XM_011521363.1:c.1071G=	XP_011519665.1:p.Gly357=
XM_005254228.3:c.972G=	XP_005254285.1:p.Gly324=
XM_011521363.2:c.1071G=	XP_011519665.1:p.Gly357=
NM_001004439.2:c.1278G= MANE Select	NP_001004439.1:p.Gly426=