Canonical Allele Identifier: CA7631869
Gene: ITGA11 HGNC NCBI

Linked Data

dbSNP Id: rs2306022

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335825C>T , CM000677.2:g.68335825C>T GRCh38
NC_000015.9:g.68628163C>T , CM000677.1:g.68628163C>T GRCh37
NC_000015.8:g.66415217C>T NCBI36
NG_046911.1:g.101336G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000315757.9:c.1297G>A MANE Select ENSP00000327290.7:p.Val433Met
ENST00000315757.8:c.1297G>A ENSP00000327290.7:p.Val433Met
ENST00000423218.6:c.1297G>A ENSP00000403392.2:p.Val433Met
ENST00000566429.1:n.197-11G>A
ENST00000569346.5:n.276G>A
NM_001004439.1:c.1297G>A NP_001004439.1:p.Val433Met
XM_005254228.2:c.991G>A XP_005254285.1:p.Val331Met
XM_011521363.1:c.1090G>A XP_011519665.1:p.Val364Met
XM_005254228.3:c.991G>A XP_005254285.1:p.Val331Met
XM_011521363.2:c.1090G>A XP_011519665.1:p.Val364Met
NM_001004439.2:c.1297G>A MANE Select NP_001004439.1:p.Val433Met