Canonical Allele Identifier: CA2634929886
Gene: CDH15 HGNC NCBI

Linked Data

gnomAD v4: 16-89179604-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179604A>G , CM000678.2:g.89179604A>G GRCh38
NC_000016.9:g.89246012A>G , CM000678.1:g.89246012A>G GRCh37
NC_000016.8:g.87773513A>G NCBI36
NG_012055.1:g.12850A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.201+30A>G MANE Select ENSP00000289746.2:n.201+30A>G
ENST00000289746.2:c.201+30A>G ENSP00000289746.2:n.201+30A>G
ENST00000521087.5:n.266+30A>G
ENST00000524089.1:n.266+30A>G
NM_004933.2:c.201+30A>G NP_004924.1:n.201+30A>G
XM_011522806.1:c.201+30A>G XP_011521108.1:n.201+30A>G
NM_004933.3:c.201+30A>G MANE Select NP_004924.1:n.201+30A>G
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