Canonical Allele Identifier: CA2270883484
Gene: AXIN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65536573_65536574delinsAG , CM000679.2:g.65536573_65536574delinsAG GRCh38
NC_000017.10:g.63532691_63532692delinsAG , CM000679.1:g.63532691_63532692delinsAG GRCh37
NC_000017.9:g.60963153_60963154delinsAG NCBI36
NG_012142.1:g.30049_30050delinsCT , LRG_296:g.30049_30050delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307078.10:c.1908-21_1908-20delinsCT MANE Select ENSP00000302625.5:n.1908-21_1908-20delinsCT
ENST00000307078.9:c.1908-21_1908-20delinsCT ENSP00000302625.5:n.1908-21_1908-20delinsCT
ENST00000375702.5:c.1713-21_1713-20delinsCT ENSP00000364854.5:n.1713-21_1713-20delinsCT
ENST00000578251.1:n.109_110delinsCT
ENST00000611991.1:c.397-7874_397-7873delinsCT ENSP00000481191.1:n.397-7874_397-7873delinsCT
ENST00000618960.4:c.1713-21_1713-20delinsCT ENSP00000478916.1:n.1713-21_1713-20delinsCT
NM_004655.3:c.1908-21_1908-20delinsCT , LRG_296t1:c.1908-21_1908-20delinsCT NP_004646.3:n.1908-21_1908-20delinsCT
XM_011525319.1:c.1908-21_1908-20delinsCT XP_011523621.1:n.1908-21_1908-20delinsCT
XM_011525320.1:c.1908-21_1908-20delinsCT XP_011523622.1:n.1908-21_1908-20delinsCT
XM_011525321.1:c.1908-21_1908-20delinsCT XP_011523623.1:n.1908-21_1908-20delinsCT
XM_011525322.1:c.1713-21_1713-20delinsCT XP_011523624.1:n.1713-21_1713-20delinsCT
NM_001363813.1:c.1713-21_1713-20delinsCT NP_001350742.1:n.1713-21_1713-20delinsCT
NM_004655.4:c.1908-21_1908-20delinsCT MANE Select NP_004646.3:n.1908-21_1908-20delinsCT
XM_011525319.2:c.1908-21_1908-20delinsCT XP_011523621.1:n.1908-21_1908-20delinsCT
XM_011525321.2:c.1908-21_1908-20delinsCT XP_011523623.1:n.1908-21_1908-20delinsCT
XM_017025192.1:c.1908-21_1908-20delinsCT XP_016880681.1:n.1908-21_1908-20delinsCT
XM_017025193.1:c.1713-21_1713-20delinsCT XP_016880682.1:n.1713-21_1713-20delinsCT