Canonical Allele Identifier: CA2629178711

Gene: ITGA11

Linked Data

• gnomAD v4: 15-68335657-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335657C>A , CM000677.2:g.68335657C>A	GRCh38
NC_000015.9:g.68627995C>A , CM000677.1:g.68627995C>A	GRCh37
NC_000015.8:g.66415049C>A	NCBI36
NG_046911.1:g.101504G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1425+40G>T MANE Select	ENSP00000327290.7:n.1425+40G>T
ENST00000315757.8:c.1425+40G>T	ENSP00000327290.7:n.1425+40G>T
ENST00000423218.6:c.1425+40G>T	ENSP00000403392.2:n.1425+40G>T
ENST00000566429.1:n.314+40G>T
ENST00000569346.5:n.404+40G>T
NM_001004439.1:c.1425+40G>T	NP_001004439.1:n.1425+40G>T
XM_005254228.2:c.1119+40G>T	XP_005254285.1:n.1119+40G>T
XM_011521363.1:c.1218+40G>T	XP_011519665.1:n.1218+40G>T
XM_005254228.3:c.1119+40G>T	XP_005254285.1:n.1119+40G>T
XM_011521363.2:c.1218+40G>T	XP_011519665.1:n.1218+40G>T
NM_001004439.2:c.1425+40G>T MANE Select	NP_001004439.1:n.1425+40G>T