Canonical Allele Identifier: CA2184934339

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335755A= , CM000677.2:g.68335755A=	GRCh38
NC_000015.9:g.68628093A= , CM000677.1:g.68628093A=	GRCh37
NC_000015.8:g.66415147A=	NCBI36
NG_046911.1:g.101406T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1367T= MANE Select	ENSP00000327290.7:p.Leu456=
ENST00000315757.8:c.1367T=	ENSP00000327290.7:p.Leu456=
ENST00000423218.6:c.1367T=	ENSP00000403392.2:p.Leu456=
ENST00000566429.1:n.256T=
ENST00000569346.5:n.346T=
NM_001004439.1:c.1367T=	NP_001004439.1:p.Leu456=
XM_005254228.2:c.1061T=	XP_005254285.1:p.Leu354=
XM_011521363.1:c.1160T=	XP_011519665.1:p.Leu387=
XM_005254228.3:c.1061T=	XP_005254285.1:p.Leu354=
XM_011521363.2:c.1160T=	XP_011519665.1:p.Leu387=
NM_001004439.2:c.1367T= MANE Select	NP_001004439.1:p.Leu456=