Canonical Allele Identifier: CA2184918470

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68304789T= , CM000677.2:g.68304789T=	GRCh38
NC_000015.9:g.68597127T= , CM000677.1:g.68597127T=	GRCh37
NC_000015.8:g.66384181T=	NCBI36
NG_046911.1:g.132372A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001004439.2:c.3382-904A= MANE Select	NP_001004439.1:n.3382-904A=
ENST00000315757.9:c.3382-904A= MANE Select	ENSP00000327290.7:n.3382-904A=
NM_001004439.1:c.3382-904A=	NP_001004439.1:n.3382-904A=
ENST00000315757.8:c.3382-904A=	ENSP00000327290.7:n.3382-904A=
ENST00000423218.6:c.3385-904A=	ENSP00000403392.2:n.3385-904A=
XM_005254228.2:c.3076-904A=	XP_005254285.1:n.3076-904A=
XM_005254228.3:c.3076-904A=	XP_005254285.1:n.3076-904A=
XM_011521363.1:c.3175-904A=	XP_011519665.1:n.3175-904A=
XM_011521363.2:c.3175-904A=	XP_011519665.1:n.3175-904A=