Canonical Allele Identifier: CA490946281

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628065G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335727G>T , CM000677.2:g.68335727G>T	GRCh38
NC_000015.9:g.68628065G>T , CM000677.1:g.68628065G>T	GRCh37
NC_000015.8:g.66415119G>T	NCBI36
NG_046911.1:g.101434C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000315757.9:c.1395C>A MANE Select	ENSP00000327290.7:p.Leu465=
ENST00000315757.8:c.1395C>A	ENSP00000327290.7:p.Leu465=
ENST00000423218.6:c.1395C>A	ENSP00000403392.2:p.Leu465=
ENST00000566429.1:n.284C>A
ENST00000569346.5:n.374C>A
NM_001004439.1:c.1395C>A	NP_001004439.1:p.Leu465=
XM_005254228.2:c.1089C>A	XP_005254285.1:p.Leu363=
XM_011521363.1:c.1188C>A	XP_011519665.1:p.Leu396=
XM_005254228.3:c.1089C>A	XP_005254285.1:p.Leu363=
XM_011521363.2:c.1188C>A	XP_011519665.1:p.Leu396=
NM_001004439.2:c.1395C>A MANE Select	NP_001004439.1:p.Leu465=