Canonical Allele Identifier: CA725656160
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs1465041953
gnomAD v3: 16-89179629-G-A
gnomAD v4: 16-89179629-G-A
MyVariant Identifiers: chr16:g.89246037G>A (hg19) chr16:g.89179629G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179629G>A , CM000678.2:g.89179629G>A GRCh38
NC_000016.9:g.89246037G>A , CM000678.1:g.89246037G>A GRCh37
NC_000016.8:g.87773538G>A NCBI36
NG_012055.1:g.12875G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.201+55G>A MANE Select ENSP00000289746.2:n.201+55G>A
ENST00000289746.2:c.201+55G>A ENSP00000289746.2:n.201+55G>A
ENST00000521087.5:n.266+55G>A
ENST00000524089.1:n.266+55G>A
NM_004933.2:c.201+55G>A NP_004924.1:n.201+55G>A
XM_011522806.1:c.201+55G>A XP_011521108.1:n.201+55G>A
NM_004933.3:c.201+55G>A MANE Select NP_004924.1:n.201+55G>A
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