Canonical Allele Identifier: CA384672375

Gene: WNT10B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48966316A>T , CM000674.2:g.48966316A>T	GRCh38
NC_000012.11:g.49360099A>T , CM000674.1:g.49360099A>T	GRCh37
NC_000012.10:g.47646366A>T	NCBI36
NG_023347.1:g.10543T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003394.4:c.949T>A MANE Select	NP_003385.2:p.Phe317Ile
ENST00000301061.9:c.949T>A MANE Select	ENSP00000301061.4:p.Phe317Ile
NM_003394.3:c.949T>A	NP_003385.2:p.Phe317Ile
ENST00000301061.8:c.949T>A	ENSP00000301061.4:p.Phe317Ile
ENST00000403957.5:c.*231T>A	ENSP00000385980.1:n.*231T>A
ENST00000407467.5:c.*231T>A	ENSP00000384691.1:n.*231T>A
XM_011538721.1:c.583T>A	XP_011537023.1:p.Phe195Ile
XM_011538722.1:c.583T>A	XP_011537024.1:p.Phe195Ile
XM_011538724.1:c.*227T>A	XP_011537026.1:n.*227T>A
XM_017019919.1:c.583T>A	XP_016875408.1:p.Phe195Ile
XM_024449179.1:c.583T>A	XP_024304947.1:p.Phe195Ile