Canonical Allele Identifier: CA2184934392

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335867T= , CM000677.2:g.68335867T=	GRCh38
NC_000015.9:g.68628205T= , CM000677.1:g.68628205T=	GRCh37
NC_000015.8:g.66415259T=	NCBI36
NG_046911.1:g.101294A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1277-22A= MANE Select	ENSP00000327290.7:n.1277-22A=
ENST00000315757.8:c.1277-22A=	ENSP00000327290.7:n.1277-22A=
ENST00000423218.6:c.1277-22A=	ENSP00000403392.2:n.1277-22A=
ENST00000566429.1:n.197-53A=
ENST00000569346.5:n.234A=
NM_001004439.1:c.1277-22A=	NP_001004439.1:n.1277-22A=
XM_005254228.2:c.971-22A=	XP_005254285.1:n.971-22A=
XM_011521363.1:c.1070-22A=	XP_011519665.1:n.1070-22A=
XM_005254228.3:c.971-22A=	XP_005254285.1:n.971-22A=
XM_011521363.2:c.1070-22A=	XP_011519665.1:n.1070-22A=
NM_001004439.2:c.1277-22A= MANE Select	NP_001004439.1:n.1277-22A=