Canonical Allele Identifier: CA397135100

Gene: CDH15

Linked Data

• MyVariant Identifiers: chr16:g.89245924T>G (hg19) ; chr16:g.89179516T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89179516T>G , CM000678.2:g.89179516T>G	GRCh38
NC_000016.9:g.89245924T>G , CM000678.1:g.89245924T>G	GRCh37
NC_000016.8:g.87773425T>G	NCBI36
NG_012055.1:g.12762T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289746.3:c.143T>G MANE Select	ENSP00000289746.2:p.Val48Gly
ENST00000289746.2:c.143T>G	ENSP00000289746.2:p.Val48Gly
ENST00000521087.5:n.208T>G
ENST00000524089.1:n.208T>G
NM_004933.2:c.143T>G	NP_004924.1:p.Val48Gly
XM_011522806.1:c.143T>G	XP_011521108.1:p.Val48Gly
NM_004933.3:c.143T>G MANE Select	NP_004924.1:p.Val48Gly