Canonical Allele Identifier: CA2184934338

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335751G= , CM000677.2:g.68335751G=	GRCh38
NC_000015.9:g.68628089G= , CM000677.1:g.68628089G=	GRCh37
NC_000015.8:g.66415143G=	NCBI36
NG_046911.1:g.101410C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1371C= MANE Select	ENSP00000327290.7:p.Phe457=
ENST00000315757.8:c.1371C=	ENSP00000327290.7:p.Phe457=
ENST00000423218.6:c.1371C=	ENSP00000403392.2:p.Phe457=
ENST00000566429.1:n.260C=
ENST00000569346.5:n.350C=
NM_001004439.1:c.1371C=	NP_001004439.1:p.Phe457=
XM_005254228.2:c.1065C=	XP_005254285.1:p.Phe355=
XM_011521363.1:c.1164C=	XP_011519665.1:p.Phe388=
XM_005254228.3:c.1065C=	XP_005254285.1:p.Phe355=
XM_011521363.2:c.1164C=	XP_011519665.1:p.Phe388=
NM_001004439.2:c.1371C= MANE Select	NP_001004439.1:p.Phe457=