Canonical Allele Identifier: CA2362679319

Gene: CTNNBL1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37712604A= , CM000682.2:g.37712604A=	GRCh38
NC_000020.10:g.36341006A= , CM000682.1:g.36341006A=	GRCh37
NC_000020.9:g.35774420A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361383.11:c.30+18452A= MANE Select	ENSP00000355050.6:n.30+18452A=
ENST00000361383.10:c.30+18452A=	ENSP00000355050.6:n.30+18452A=
ENST00000405275.6:c.-152-14698A=	ENSP00000384355.2:n.-152-14698A=
ENST00000447935.3:c.-52+17571A=	ENSP00000394464.1:n.-52+17571A=
ENST00000621317.4:c.30+18452A=	ENSP00000478532.1:n.30+18452A=
ENST00000628103.2:c.-152-14698A=	ENSP00000487198.1:n.-152-14698A=
NM_001281495.1:c.-152-14698A=	NP_001268424.1:n.-152-14698A=
NM_030877.4:c.30+18452A=	NP_110517.2:n.30+18452A=
XM_024451947.1:c.-52+17571A=	XP_024307715.1:n.-52+17571A=
NM_030877.5:c.30+18452A= MANE Select	NP_110517.2:n.30+18452A=
NM_001281495.2:c.-152-14698A=	NP_001268424.1:n.-152-14698A=