Canonical Allele Identifier: CA1410268400

Gene: WWTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149532802T= , CM000665.2:g.149532802T=	GRCh38
NC_000003.11:g.149250589T= , CM000665.1:g.149250589T=	GRCh37
NC_000003.10:g.150733279T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015472.6:c.772-4833A= MANE Select	NP_056287.1:n.772-4833A=
ENST00000360632.8:c.772-4833A= MANE Select	ENSP00000353847.3:n.772-4833A=
NM_001168278.1:c.772-4833A=	NP_001161750.1:n.772-4833A=
NM_001168278.2:c.772-4833A=	NP_001161750.1:n.772-4833A=
NM_001168278.3:c.772-4833A=	NP_001161750.1:n.772-4833A=
NM_001168280.1:c.772-4833A=	NP_001161752.1:n.772-4833A=
NM_001168280.2:c.772-4833A=	NP_001161752.1:n.772-4833A=
NM_001168280.3:c.772-4833A=	NP_001161752.1:n.772-4833A=
NM_001348362.1:c.772-4833A=	NP_001335291.1:n.772-4833A=
NM_001348362.2:c.772-4833A=	NP_001335291.1:n.772-4833A=
NM_015472.4:c.772-4833A=	NP_056287.1:n.772-4833A=
NM_015472.5:c.772-4833A=	NP_056287.1:n.772-4833A=
ENST00000360632.7:c.772-4833A=	ENSP00000353847.3:n.772-4833A=
ENST00000465804.5:c.772-4833A=	ENSP00000419465.1:n.772-4833A=
ENST00000467467.5:c.772-4833A=	ENSP00000419234.1:n.772-4833A=
ENST00000471586.5:c.47-4833A=
ENST00000472417.1:c.346-4833A=	ENSP00000417339.1:n.346-4833A=
ENST00000485244.1:n.106-4833A=
ENST00000494754.1:c.52-4833A=
XM_011512661.1:c.772-4833A=	XP_011510963.1:n.772-4833A=
XM_017006122.1:c.772-4833A=	XP_016861611.1:n.772-4833A=