Canonical Allele Identifier: CA8238707
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs776191977
ExAC: 16:89245971 C / A
gnomAD v2: 16-89245971-C-A
gnomAD v4: 16-89179563-C-A
COSMIC: COSM6080283
MyVariant Identifiers: chr16:g.89245971C>A (hg19) chr16:g.89179563C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179563C>A , CM000678.2:g.89179563C>A GRCh38
NC_000016.9:g.89245971C>A , CM000678.1:g.89245971C>A GRCh37
NC_000016.8:g.87773472C>A NCBI36
NG_012055.1:g.12809C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000289746.3:c.190C>A MANE Select ENSP00000289746.2:p.Pro64Thr
ENST00000289746.2:c.190C>A ENSP00000289746.2:p.Pro64Thr
ENST00000521087.5:n.255C>A
ENST00000524089.1:n.255C>A
NM_004933.2:c.190C>A NP_004924.1:p.Pro64Thr
XM_011522806.1:c.190C>A XP_011521108.1:p.Pro64Thr
NM_004933.3:c.190C>A MANE Select NP_004924.1:p.Pro64Thr
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