Canonical Allele Identifier: CA397134966
Gene: CDH15 HGNC NCBI

Linked Data

gnomAD v4: 16-89179496-C-A
MyVariant Identifiers: chr16:g.89245904C>A (hg19) chr16:g.89179496C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179496C>A , CM000678.2:g.89179496C>A GRCh38
NC_000016.9:g.89245904C>A , CM000678.1:g.89245904C>A GRCh37
NC_000016.8:g.87773405C>A NCBI36
NG_012055.1:g.12742C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.123C>A MANE Select ENSP00000289746.2:p.Ser41Arg
ENST00000289746.2:c.123C>A ENSP00000289746.2:p.Ser41Arg
ENST00000521087.5:n.188C>A
ENST00000524089.1:n.188C>A
NM_004933.2:c.123C>A NP_004924.1:p.Ser41Arg
XM_011522806.1:c.123C>A XP_011521108.1:p.Ser41Arg
NM_004933.3:c.123C>A MANE Select NP_004924.1:p.Ser41Arg
Search 100 bp 5'
Search 100 bp 3'