Canonical Allele Identifier: CA2270883408

Gene: AXIN2

Linked Data

• dbSNP Id: rs2043919173

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536466_65536467delinsTG , CM000679.2:g.65536466_65536467delinsTG	GRCh38
NC_000017.10:g.63532584_63532585delinsTG , CM000679.1:g.63532584_63532585delinsTG	GRCh37
NC_000017.9:g.60963046_60963047delinsTG	NCBI36
NG_012142.1:g.30156_30157delinsCA , LRG_296:g.30156_30157delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.1994_1995delinsCA MANE Select	ENSP00000302625.5:p.Gly665Ala
ENST00000307078.9:c.1994_1995delinsCA	ENSP00000302625.5:p.Gly665Ala
ENST00000375702.5:c.1799_1800delinsCA	ENSP00000364854.5:p.Gly600Ala
ENST00000578251.1:n.216_217delinsCA
ENST00000611991.1:c.397-7767_397-7766delinsCA	ENSP00000481191.1:n.397-7767_397-7766delinsCA
ENST00000618960.4:c.1799_1800delinsCA	ENSP00000478916.1:p.Gly600Ala
NM_004655.3:c.1994_1995delinsCA , LRG_296t1:c.1994_1995delinsCA	NP_004646.3:p.Gly665Ala
XM_011525319.1:c.1994_1995delinsCA	XP_011523621.1:p.Gly665Ala
XM_011525320.1:c.1994_1995delinsCA	XP_011523622.1:p.Gly665Ala
XM_011525321.1:c.1994_1995delinsCA	XP_011523623.1:p.Gly665Ala
XM_011525322.1:c.1799_1800delinsCA	XP_011523624.1:p.Gly600Ala
NM_001363813.1:c.1799_1800delinsCA	NP_001350742.1:p.Gly600Ala
NM_004655.4:c.1994_1995delinsCA MANE Select	NP_004646.3:p.Gly665Ala
XM_011525319.2:c.1994_1995delinsCA	XP_011523621.1:p.Gly665Ala
XM_011525321.2:c.1994_1995delinsCA	XP_011523623.1:p.Gly665Ala
XM_017025192.1:c.1994_1995delinsCA	XP_016880681.1:p.Gly665Ala
XM_017025193.1:c.1799_1800delinsCA	XP_016880682.1:p.Gly600Ala