Canonical Allele Identifier: CA392977663

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628038C>A (hg19) ; chr15:g.68335700C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335700C>A , CM000677.2:g.68335700C>A	GRCh38
NC_000015.9:g.68628038C>A , CM000677.1:g.68628038C>A	GRCh37
NC_000015.8:g.66415092C>A	NCBI36
NG_046911.1:g.101461G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315757.9:c.1422G>T MANE Select	ENSP00000327290.7:p.Gln474His
ENST00000315757.8:c.1422G>T	ENSP00000327290.7:p.Gln474His
ENST00000423218.6:c.1422G>T	ENSP00000403392.2:p.Gln474His
ENST00000566429.1:n.311G>T
ENST00000569346.5:n.401G>T
NM_001004439.1:c.1422G>T	NP_001004439.1:p.Gln474His
XM_005254228.2:c.1116G>T	XP_005254285.1:p.Gln372His
XM_011521363.1:c.1215G>T	XP_011519665.1:p.Gln405His
XM_005254228.3:c.1116G>T	XP_005254285.1:p.Gln372His
XM_011521363.2:c.1215G>T	XP_011519665.1:p.Gln405His
NM_001004439.2:c.1422G>T MANE Select	NP_001004439.1:p.Gln474His