Canonical Allele Identifier: CA2362703841

Gene: CTNNBL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37771178G= , CM000682.2:g.37771178G=	GRCh38
NC_000020.10:g.36399580G= , CM000682.1:g.36399580G=	GRCh37
NC_000020.9:g.35832994G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030877.5:c.750+3134G= MANE Select	NP_110517.2:n.750+3134G=
ENST00000361383.11:c.750+3134G= MANE Select	ENSP00000355050.6:n.750+3134G=
NM_001281495.1:c.669+3134G=	NP_001268424.1:n.669+3134G=
NM_001281495.2:c.669+3134G=	NP_001268424.1:n.669+3134G=
NM_030877.4:c.750+3134G=	NP_110517.2:n.750+3134G=
ENST00000361383.10:c.750+3134G=	ENSP00000355050.6:n.750+3134G=
ENST00000373473.5:c.189+3134G=	ENSP00000362572.1:n.189+3134G=
ENST00000405275.6:c.669+3134G=	ENSP00000384355.2:n.669+3134G=
ENST00000473857.5:n.1834+3134G=
ENST00000621317.4:c.765+3134G=	ENSP00000478532.1:n.765+3134G=
ENST00000628103.2:c.669+3134G=	ENSP00000487198.1:n.669+3134G=
XM_011528917.1:c.420+3134G=	XP_011527219.1:n.420+3134G=
XM_011528917.2:c.420+3134G=	XP_011527219.1:n.420+3134G=
XM_024451947.1:c.669+3134G=	XP_024307715.1:n.669+3134G=