Canonical Allele Identifier: CA497144479

Gene: CDH15

Linked Data

• dbSNP Id: rs1567771162
• gnomAD v4: 16-89179463-C-T
• MyVariant Identifiers: chr16:g.89245871C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89179463C>T , CM000678.2:g.89179463C>T	GRCh38
NC_000016.9:g.89245871C>T , CM000678.1:g.89245871C>T	GRCh37
NC_000016.8:g.87773372C>T	NCBI36
NG_012055.1:g.12709C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289746.3:c.90C>T MANE Select	ENSP00000289746.2:p.Thr30=
ENST00000289746.2:c.90C>T	ENSP00000289746.2:p.Thr30=
ENST00000521087.5:n.155C>T
ENST00000524089.1:n.155C>T
NM_004933.2:c.90C>T	NP_004924.1:p.Thr30=
XM_011522806.1:c.90C>T	XP_011521108.1:p.Thr30=
NM_004933.3:c.90C>T MANE Select	NP_004924.1:p.Thr30=