Canonical Allele Identifier: CA397135086
Gene: CDH15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.89245923G>A (hg19) chr16:g.89179515G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179515G>A , CM000678.2:g.89179515G>A GRCh38
NC_000016.9:g.89245923G>A , CM000678.1:g.89245923G>A GRCh37
NC_000016.8:g.87773424G>A NCBI36
NG_012055.1:g.12761G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.142G>A MANE Select ENSP00000289746.2:p.Val48Ile
ENST00000289746.2:c.142G>A ENSP00000289746.2:p.Val48Ile
ENST00000521087.5:n.207G>A
ENST00000524089.1:n.207G>A
NM_004933.2:c.142G>A NP_004924.1:p.Val48Ile
XM_011522806.1:c.142G>A XP_011521108.1:p.Val48Ile
NM_004933.3:c.142G>A MANE Select NP_004924.1:p.Val48Ile
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