Canonical Allele Identifier: CA2184934325
Gene: ITGA11 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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