Canonical Allele Identifier: CA2184934326
Gene: ITGA11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335731C= , CM000677.2:g.68335731C= GRCh38
NC_000015.9:g.68628069C= , CM000677.1:g.68628069C= GRCh37
NC_000015.8:g.66415123C= NCBI36
NG_046911.1:g.101430G=

Transcript Alleles

HGVS Amino-acid change
ENST00000315757.9:c.1391G= MANE Select ENSP00000327290.7:p.Ser464=
ENST00000315757.8:c.1391G= ENSP00000327290.7:p.Ser464=
ENST00000423218.6:c.1391G= ENSP00000403392.2:p.Ser464=
ENST00000566429.1:n.280G=
ENST00000569346.5:n.370G=
NM_001004439.1:c.1391G= NP_001004439.1:p.Ser464=
XM_005254228.2:c.1085G= XP_005254285.1:p.Ser362=
XM_011521363.1:c.1184G= XP_011519665.1:p.Ser395=
XM_005254228.3:c.1085G= XP_005254285.1:p.Ser362=
XM_011521363.2:c.1184G= XP_011519665.1:p.Ser395=
NM_001004439.2:c.1391G= MANE Select NP_001004439.1:p.Ser464=