Canonical Allele Identifier: CA2270891840
Gene: AXIN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65553422A= , CM000679.2:g.65553422A= GRCh38
NC_000017.10:g.63549540A= , CM000679.1:g.63549540A= GRCh37
NC_000017.9:g.60980002A= NCBI36
NG_012142.1:g.13201T= , LRG_296:g.13201T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307078.10:c.816-3762T= MANE Select ENSP00000302625.5:n.816-3762T=
ENST00000307078.9:c.816-3762T= ENSP00000302625.5:n.816-3762T=
ENST00000375702.5:c.816-3762T= ENSP00000364854.5:n.816-3762T=
ENST00000577662.1:c.1131-3762T=
ENST00000611991.1:c.396+4803T= ENSP00000481191.1:n.396+4803T=
ENST00000618960.4:c.816-3762T= ENSP00000478916.1:n.816-3762T=
NM_004655.3:c.816-3762T= , LRG_296t1:c.816-3762T= NP_004646.3:n.816-3762T=
XM_011525319.1:c.816-3762T= XP_011523621.1:n.816-3762T=
XM_011525320.1:c.816-3762T= XP_011523622.1:n.816-3762T=
XM_011525321.1:c.816-3762T= XP_011523623.1:n.816-3762T=
XM_011525322.1:c.816-3762T= XP_011523624.1:n.816-3762T=
NM_001363813.1:c.816-3762T= NP_001350742.1:n.816-3762T=
NM_004655.4:c.816-3762T= MANE Select NP_004646.3:n.816-3762T=
XM_011525319.2:c.816-3762T= XP_011523621.1:n.816-3762T=
XM_011525321.2:c.816-3762T= XP_011523623.1:n.816-3762T=
XM_017025192.1:c.816-3762T= XP_016880681.1:n.816-3762T=
XM_017025193.1:c.816-3762T= XP_016880682.1:n.816-3762T=