Canonical Allele Identifier: CA497144535

Gene: CDH15

Linked Data

• MyVariant Identifiers: chr16:g.89245946C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89179538C>G , CM000678.2:g.89179538C>G	GRCh38
NC_000016.9:g.89245946C>G , CM000678.1:g.89245946C>G	GRCh37
NC_000016.8:g.87773447C>G	NCBI36
NG_012055.1:g.12784C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289746.3:c.165C>G MANE Select	ENSP00000289746.2:p.Ser55=
ENST00000289746.2:c.165C>G	ENSP00000289746.2:p.Ser55=
ENST00000521087.5:n.230C>G
ENST00000524089.1:n.230C>G
NM_004933.2:c.165C>G	NP_004924.1:p.Ser55=
XM_011522806.1:c.165C>G	XP_011521108.1:p.Ser55=
NM_004933.3:c.165C>G MANE Select	NP_004924.1:p.Ser55=