Canonical Allele Identifier: CA397134851
Gene: CDH15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179474G>T , CM000678.2:g.89179474G>T GRCh38
NC_000016.9:g.89245882G>T , CM000678.1:g.89245882G>T GRCh37
NC_000016.8:g.87773383G>T NCBI36
NG_012055.1:g.12720G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.101G>T MANE Select ENSP00000289746.2:p.Trp34Leu
ENST00000289746.2:c.101G>T ENSP00000289746.2:p.Trp34Leu
ENST00000521087.5:n.166G>T
ENST00000524089.1:n.166G>T
NM_004933.2:c.101G>T NP_004924.1:p.Trp34Leu
XM_011522806.1:c.101G>T XP_011521108.1:p.Trp34Leu
NM_004933.3:c.101G>T MANE Select NP_004924.1:p.Trp34Leu