Canonical Allele Identifier: CA397134755
Gene: CDH15 HGNC NCBI

Linked Data

dbSNP Id: rs1597303100
MyVariant Identifiers: chr16:g.89245866A>C (hg19) chr16:g.89179458A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89179458A>C , CM000678.2:g.89179458A>C GRCh38
NC_000016.9:g.89245866A>C , CM000678.1:g.89245866A>C GRCh37
NC_000016.8:g.87773367A>C NCBI36
NG_012055.1:g.12704A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000289746.3:c.85A>C MANE Select ENSP00000289746.2:p.Thr29Pro
ENST00000289746.2:c.85A>C ENSP00000289746.2:p.Thr29Pro
ENST00000521087.5:n.150A>C
ENST00000524089.1:n.150A>C
NM_004933.2:c.85A>C NP_004924.1:p.Thr29Pro
XM_011522806.1:c.85A>C XP_011521108.1:p.Thr29Pro
NM_004933.3:c.85A>C MANE Select NP_004924.1:p.Thr29Pro
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