Canonical Allele Identifier: CA497144513

Gene: CDH15

Linked Data

• MyVariant Identifiers: chr16:g.89245913G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89179505G>C , CM000678.2:g.89179505G>C	GRCh38
NC_000016.9:g.89245913G>C , CM000678.1:g.89245913G>C	GRCh37
NC_000016.8:g.87773414G>C	NCBI36
NG_012055.1:g.12751G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289746.3:c.132G>C MANE Select	ENSP00000289746.2:p.Arg44=
ENST00000289746.2:c.132G>C	ENSP00000289746.2:p.Arg44=
ENST00000521087.5:n.197G>C
ENST00000524089.1:n.197G>C
NM_004933.2:c.132G>C	NP_004924.1:p.Arg44=
XM_011522806.1:c.132G>C	XP_011521108.1:p.Arg44=
NM_004933.3:c.132G>C MANE Select	NP_004924.1:p.Arg44=