Canonical Allele Identifier: CA397135217
Gene: CDH15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179537C>T , CM000678.2:g.89179537C>T GRCh38
NC_000016.9:g.89245945C>T , CM000678.1:g.89245945C>T GRCh37
NC_000016.8:g.87773446C>T NCBI36
NG_012055.1:g.12783C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.164C>T MANE Select ENSP00000289746.2:p.Ser55Phe
ENST00000289746.2:c.164C>T ENSP00000289746.2:p.Ser55Phe
ENST00000521087.5:n.229C>T
ENST00000524089.1:n.229C>T
NM_004933.2:c.164C>T NP_004924.1:p.Ser55Phe
XM_011522806.1:c.164C>T XP_011521108.1:p.Ser55Phe
NM_004933.3:c.164C>T MANE Select NP_004924.1:p.Ser55Phe