Canonical Allele Identifier: CA497144476

Gene: CDH15

Linked Data

• MyVariant Identifiers: chr16:g.89245868C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89179460C>T , CM000678.2:g.89179460C>T	GRCh38
NC_000016.9:g.89245868C>T , CM000678.1:g.89245868C>T	GRCh37
NC_000016.8:g.87773369C>T	NCBI36
NG_012055.1:g.12706C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289746.3:c.87C>T MANE Select	ENSP00000289746.2:p.Thr29=
ENST00000289746.2:c.87C>T	ENSP00000289746.2:p.Thr29=
ENST00000521087.5:n.152C>T
ENST00000524089.1:n.152C>T
NM_004933.2:c.87C>T	NP_004924.1:p.Thr29=
XM_011522806.1:c.87C>T	XP_011521108.1:p.Thr29=
NM_004933.3:c.87C>T MANE Select	NP_004924.1:p.Thr29=