Canonical Allele Identifier: CA2241534782
Gene: CDH15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179514G= , CM000678.2:g.89179514G= GRCh38
NC_000016.9:g.89245922G= , CM000678.1:g.89245922G= GRCh37
NC_000016.8:g.87773423G= NCBI36
NG_012055.1:g.12760G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.141G= MANE Select ENSP00000289746.2:p.Trp47=
ENST00000289746.2:c.141G= ENSP00000289746.2:p.Trp47=
ENST00000521087.5:n.206G=
ENST00000524089.1:n.206G=
NM_004933.2:c.141G= NP_004924.1:p.Trp47=
XM_011522806.1:c.141G= XP_011521108.1:p.Trp47=
NM_004933.3:c.141G= MANE Select NP_004924.1:p.Trp47=