Canonical Allele Identifier: CA397134859
Gene: CDH15 HGNC NCBI

Linked Data

gnomAD v4: 16-89179476-C-A
MyVariant Identifiers: chr16:g.89245884C>A (hg19) chr16:g.89179476C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179476C>A , CM000678.2:g.89179476C>A GRCh38
NC_000016.9:g.89245884C>A , CM000678.1:g.89245884C>A GRCh37
NC_000016.8:g.87773385C>A NCBI36
NG_012055.1:g.12722C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.103C>A MANE Select ENSP00000289746.2:p.Arg35Ser
ENST00000289746.2:c.103C>A ENSP00000289746.2:p.Arg35Ser
ENST00000521087.5:n.168C>A
ENST00000524089.1:n.168C>A
NM_004933.2:c.103C>A NP_004924.1:p.Arg35Ser
XM_011522806.1:c.103C>A XP_011521108.1:p.Arg35Ser
NM_004933.3:c.103C>A MANE Select NP_004924.1:p.Arg35Ser
Search 100 bp 5'
Search 100 bp 3'