Canonical Allele Identifier: CA2270883299

Gene: AXIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536324G= , CM000679.2:g.65536324G=	GRCh38
NC_000017.10:g.63532442G= , CM000679.1:g.63532442G=	GRCh37
NC_000017.9:g.60962904G=	NCBI36
NG_012142.1:g.30299C= , LRG_296:g.30299C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.2137C= MANE Select	ENSP00000302625.5:p.Gln713=
ENST00000307078.9:c.2137C=	ENSP00000302625.5:p.Gln713=
ENST00000375702.5:c.1942C=	ENSP00000364854.5:p.Gln648=
ENST00000578251.1:n.359C=
ENST00000611991.1:c.397-7624C=	ENSP00000481191.1:n.397-7624C=
ENST00000618960.4:c.1942C=	ENSP00000478916.1:p.Gln648=
NM_004655.3:c.2137C= , LRG_296t1:c.2137C=	NP_004646.3:p.Gln713=
XM_011525319.1:c.2137C=	XP_011523621.1:p.Gln713=
XM_011525320.1:c.2137C=	XP_011523622.1:p.Gln713=
XM_011525321.1:c.2137C=	XP_011523623.1:p.Gln713=
XM_011525322.1:c.1942C=	XP_011523624.1:p.Gln648=
NM_001363813.1:c.1942C=	NP_001350742.1:p.Gln648=
NM_004655.4:c.2137C= MANE Select	NP_004646.3:p.Gln713=
XM_011525319.2:c.2137C=	XP_011523621.1:p.Gln713=
XM_011525321.2:c.2137C=	XP_011523623.1:p.Gln713=
XM_017025192.1:c.2137C=	XP_016880681.1:p.Gln713=
XM_017025193.1:c.1942C=	XP_016880682.1:p.Gln648=