Canonical Allele Identifier: CA392977736
Gene: ITGA11 HGNC NCBI

Linked Data

dbSNP Id: rs776834465

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335735G>C , CM000677.2:g.68335735G>C GRCh38
NC_000015.9:g.68628073G>C , CM000677.1:g.68628073G>C GRCh37
NC_000015.8:g.66415127G>C NCBI36
NG_046911.1:g.101426C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315757.9:c.1387C>G MANE Select ENSP00000327290.7:p.Arg463Gly
ENST00000315757.8:c.1387C>G ENSP00000327290.7:p.Arg463Gly
ENST00000423218.6:c.1387C>G ENSP00000403392.2:p.Arg463Gly
ENST00000566429.1:n.276C>G
ENST00000569346.5:n.366C>G
NM_001004439.1:c.1387C>G NP_001004439.1:p.Arg463Gly
XM_005254228.2:c.1081C>G XP_005254285.1:p.Arg361Gly
XM_011521363.1:c.1180C>G XP_011519665.1:p.Arg394Gly
XM_005254228.3:c.1081C>G XP_005254285.1:p.Arg361Gly
XM_011521363.2:c.1180C>G XP_011519665.1:p.Arg394Gly
NM_001004439.2:c.1387C>G MANE Select NP_001004439.1:p.Arg463Gly