Canonical Allele Identifier: CA392977730
Gene: ITGA11 HGNC NCBI

Linked Data

dbSNP Id: rs1254942640

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000315757.9:c.1391G>A MANE Select ENSP00000327290.7:p.Ser464Asn
ENST00000315757.8:c.1391G>A ENSP00000327290.7:p.Ser464Asn
ENST00000423218.6:c.1391G>A ENSP00000403392.2:p.Ser464Asn
ENST00000566429.1:n.280G>A
ENST00000569346.5:n.370G>A
NM_001004439.1:c.1391G>A NP_001004439.1:p.Ser464Asn
XM_005254228.2:c.1085G>A XP_005254285.1:p.Ser362Asn
XM_011521363.1:c.1184G>A XP_011519665.1:p.Ser395Asn
XM_005254228.3:c.1085G>A XP_005254285.1:p.Ser362Asn
XM_011521363.2:c.1184G>A XP_011519665.1:p.Ser395Asn
NM_001004439.2:c.1391G>A MANE Select NP_001004439.1:p.Ser464Asn