Canonical Allele Identifier: CA497144524

Gene: CDH15

Linked Data

• MyVariant Identifiers: chr16:g.89245931C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89179523C>A , CM000678.2:g.89179523C>A	GRCh38
NC_000016.9:g.89245931C>A , CM000678.1:g.89245931C>A	GRCh37
NC_000016.8:g.87773432C>A	NCBI36
NG_012055.1:g.12769C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289746.3:c.150C>A MANE Select	ENSP00000289746.2:p.Pro50=
ENST00000289746.2:c.150C>A	ENSP00000289746.2:p.Pro50=
ENST00000521087.5:n.215C>A
ENST00000524089.1:n.215C>A
NM_004933.2:c.150C>A	NP_004924.1:p.Pro50=
XM_011522806.1:c.150C>A	XP_011521108.1:p.Pro50=
NM_004933.3:c.150C>A MANE Select	NP_004924.1:p.Pro50=