Canonical Allele Identifier: CA8238673
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs766936067
ExAC: 16:89245874 G / C
gnomAD v2: 16-89245874-G-C
gnomAD v4: 16-89179466-G-C
MyVariant Identifiers: chr16:g.89245874G>C (hg19) chr16:g.89179466G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179466G>C , CM000678.2:g.89179466G>C GRCh38
NC_000016.9:g.89245874G>C , CM000678.1:g.89245874G>C GRCh37
NC_000016.8:g.87773375G>C NCBI36
NG_012055.1:g.12712G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.93G>C MANE Select ENSP00000289746.2:p.Leu31=
ENST00000289746.2:c.93G>C ENSP00000289746.2:p.Leu31=
ENST00000521087.5:n.158G>C
ENST00000524089.1:n.158G>C
NM_004933.2:c.93G>C NP_004924.1:p.Leu31=
XM_011522806.1:c.93G>C XP_011521108.1:p.Leu31=
NM_004933.3:c.93G>C MANE Select NP_004924.1:p.Leu31=
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