Canonical Allele Identifier: CA8238696
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs748683653

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179508G>A , CM000678.2:g.89179508G>A GRCh38
NC_000016.9:g.89245916G>A , CM000678.1:g.89245916G>A GRCh37
NC_000016.8:g.87773417G>A NCBI36
NG_012055.1:g.12754G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.135G>A MANE Select ENSP00000289746.2:p.Arg45=
ENST00000289746.2:c.135G>A ENSP00000289746.2:p.Arg45=
ENST00000521087.5:n.200G>A
ENST00000524089.1:n.200G>A
NM_004933.2:c.135G>A NP_004924.1:p.Arg45=
XM_011522806.1:c.135G>A XP_011521108.1:p.Arg45=
NM_004933.3:c.135G>A MANE Select NP_004924.1:p.Arg45=