Canonical Allele Identifier: CA384670687

Gene: WNT10B

Linked Data

• MyVariant Identifiers: chr12:g.49359883T>A (hg19) ; chr12:g.48966100T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966100T>A , CM000674.2:g.48966100T>A	GRCh38
NC_000012.11:g.49359883T>A , CM000674.1:g.49359883T>A	GRCh37
NC_000012.10:g.47646150T>A	NCBI36
NG_023347.1:g.10759A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301061.9:c.1165A>T MANE Select	ENSP00000301061.4:p.Lys389Ter
ENST00000301061.8:c.1165A>T	ENSP00000301061.4:p.Lys389Ter
ENST00000403957.5:c.*447A>T	ENSP00000385980.1:n.*447A>T
ENST00000407467.5:c.*447A>T	ENSP00000384691.1:n.*447A>T
NM_003394.3:c.1165A>T	NP_003385.2:p.Lys389Ter
XM_011538721.1:c.799A>T	XP_011537023.1:p.Lys267Ter
XM_011538722.1:c.799A>T	XP_011537024.1:p.Lys267Ter
XM_017019919.1:c.799A>T	XP_016875408.1:p.Lys267Ter
XM_024449179.1:c.799A>T	XP_024304947.1:p.Lys267Ter
NM_003394.4:c.1165A>T MANE Select	NP_003385.2:p.Lys389Ter