Canonical Allele Identifier: CA8238692
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs763672448

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179502G>A , CM000678.2:g.89179502G>A GRCh38
NC_000016.9:g.89245910G>A , CM000678.1:g.89245910G>A GRCh37
NC_000016.8:g.87773411G>A NCBI36
NG_012055.1:g.12748G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.129G>A MANE Select ENSP00000289746.2:p.Val43=
ENST00000289746.2:c.129G>A ENSP00000289746.2:p.Val43=
ENST00000521087.5:n.194G>A
ENST00000524089.1:n.194G>A
NM_004933.2:c.129G>A NP_004924.1:p.Val43=
XM_011522806.1:c.129G>A XP_011521108.1:p.Val43=
NM_004933.3:c.129G>A MANE Select NP_004924.1:p.Val43=