Canonical Allele Identifier: CA2241534914
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs1915331694
gnomAD v4: 16-89179620-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179620C>A , CM000678.2:g.89179620C>A GRCh38
NC_000016.9:g.89246028C>A , CM000678.1:g.89246028C>A GRCh37
NC_000016.8:g.87773529C>A NCBI36
NG_012055.1:g.12866C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.201+46C>A MANE Select ENSP00000289746.2:n.201+46C>A
ENST00000289746.2:c.201+46C>A ENSP00000289746.2:n.201+46C>A
ENST00000521087.5:n.266+46C>A
ENST00000524089.1:n.266+46C>A
NM_004933.2:c.201+46C>A NP_004924.1:n.201+46C>A
XM_011522806.1:c.201+46C>A XP_011521108.1:n.201+46C>A
NM_004933.3:c.201+46C>A MANE Select NP_004924.1:n.201+46C>A
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