Canonical Allele Identifier: CA7631849
Gene: ITGA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 725622
ClinVar RCV Id: RCV000899714
dbSNP Id: rs61729766
ExAC: 15:68628072 C / T
gnomAD v2: 15-68628072-C-T
gnomAD v3: 15-68335734-C-T
gnomAD v4: 15-68335734-C-T
COSMIC: COSM1210973
MyVariant Identifiers: chr15:g.68628072C>T (hg19) chr15:g.68335734C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.68335734C>T , CM000677.2:g.68335734C>T GRCh38
NC_000015.9:g.68628072C>T , CM000677.1:g.68628072C>T GRCh37
NC_000015.8:g.66415126C>T NCBI36
NG_046911.1:g.101427G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315757.9:c.1388G>A MANE Select ENSP00000327290.7:p.Arg463Gln
ENST00000315757.8:c.1388G>A ENSP00000327290.7:p.Arg463Gln
ENST00000423218.6:c.1388G>A ENSP00000403392.2:p.Arg463Gln
ENST00000566429.1:n.277G>A
ENST00000569346.5:n.367G>A
NM_001004439.1:c.1388G>A NP_001004439.1:p.Arg463Gln
XM_005254228.2:c.1082G>A XP_005254285.1:p.Arg361Gln
XM_011521363.1:c.1181G>A XP_011519665.1:p.Arg394Gln
XM_005254228.3:c.1082G>A XP_005254285.1:p.Arg361Gln
XM_011521363.2:c.1181G>A XP_011519665.1:p.Arg394Gln
NM_001004439.2:c.1388G>A MANE Select NP_001004439.1:p.Arg463Gln
Search 100 bp 5'
Search 100 bp 3'