Canonical Allele Identifier: CA397135151
Gene: CDH15 HGNC NCBI

Linked Data

gnomAD v4: 16-89179527-A-G
MyVariant Identifiers: chr16:g.89245935A>G (hg19) chr16:g.89179527A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179527A>G , CM000678.2:g.89179527A>G GRCh38
NC_000016.9:g.89245935A>G , CM000678.1:g.89245935A>G GRCh37
NC_000016.8:g.87773436A>G NCBI36
NG_012055.1:g.12773A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.154A>G MANE Select ENSP00000289746.2:p.Ile52Val
ENST00000289746.2:c.154A>G ENSP00000289746.2:p.Ile52Val
ENST00000521087.5:n.219A>G
ENST00000524089.1:n.219A>G
NM_004933.2:c.154A>G NP_004924.1:p.Ile52Val
XM_011522806.1:c.154A>G XP_011521108.1:p.Ile52Val
NM_004933.3:c.154A>G MANE Select NP_004924.1:p.Ile52Val
Search 100 bp 5'
Search 100 bp 3'