Canonical Allele Identifier: CA2184934397

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335876G= , CM000677.2:g.68335876G=	GRCh38
NC_000015.9:g.68628214G= , CM000677.1:g.68628214G=	GRCh37
NC_000015.8:g.66415268G=	NCBI36
NG_046911.1:g.101285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1277-31C= MANE Select	ENSP00000327290.7:n.1277-31C=
ENST00000315757.8:c.1277-31C=	ENSP00000327290.7:n.1277-31C=
ENST00000423218.6:c.1277-31C=	ENSP00000403392.2:n.1277-31C=
ENST00000566429.1:n.197-62C=
ENST00000569346.5:n.225C=
NM_001004439.1:c.1277-31C=	NP_001004439.1:n.1277-31C=
XM_005254228.2:c.971-31C=	XP_005254285.1:n.971-31C=
XM_011521363.1:c.1070-31C=	XP_011519665.1:n.1070-31C=
XM_005254228.3:c.971-31C=	XP_005254285.1:n.971-31C=
XM_011521363.2:c.1070-31C=	XP_011519665.1:n.1070-31C=
NM_001004439.2:c.1277-31C= MANE Select	NP_001004439.1:n.1277-31C=