Canonical Allele Identifier: CA127320
Gene: CDH15 HGNC NCBI

Linked Data

ClinVar Variation Id: 17643
dbSNP Id: rs121434540

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89180272C>T , CM000678.2:g.89180272C>T GRCh38
NC_000016.9:g.89246680C>T , CM000678.1:g.89246680C>T GRCh37
NC_000016.8:g.87774181C>T NCBI36
NG_012055.1:g.13518C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000289746.3:c.274C>T MANE Select ENSP00000289746.2:p.Arg92Trp
ENST00000289746.2:c.274C>T ENSP00000289746.2:p.Arg92Trp
ENST00000521087.5:n.266+698C>T
ENST00000524089.1:n.339C>T
NM_004933.2:c.274C>T NP_004924.1:p.Arg92Trp
XM_011522806.1:c.274C>T XP_011521108.1:p.Arg92Trp
NM_004933.3:c.274C>T MANE Select NP_004924.1:p.Arg92Trp