Canonical Allele Identifier: CA2843625558

Gene: ITGA11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335646T>A , CM000677.2:g.68335646T>A	GRCh38
NC_000015.9:g.68627984T>A , CM000677.1:g.68627984T>A	GRCh37
NC_000015.8:g.66415038T>A	NCBI36
NG_046911.1:g.101515A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+51A>T MANE Select	ENSP00000327290.7:n.1425+51A>T
ENST00000315757.8:c.1425+51A>T	ENSP00000327290.7:n.1425+51A>T
ENST00000423218.6:c.1425+51A>T	ENSP00000403392.2:n.1425+51A>T
ENST00000566429.1:n.314+51A>T
ENST00000569346.5:n.404+51A>T
NM_001004439.1:c.1425+51A>T	NP_001004439.1:n.1425+51A>T
XM_005254228.2:c.1119+51A>T	XP_005254285.1:n.1119+51A>T
XM_011521363.1:c.1218+51A>T	XP_011519665.1:n.1218+51A>T
XM_005254228.3:c.1119+51A>T	XP_005254285.1:n.1119+51A>T
XM_011521363.2:c.1218+51A>T	XP_011519665.1:n.1218+51A>T
NM_001004439.2:c.1425+51A>T MANE Select	NP_001004439.1:n.1425+51A>T