Canonical Allele Identifier: CA298415
Gene: AXIN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65536443_65536454del , CM000679.2:g.65536443_65536454del GRCh38
NC_000017.10:g.63532561_63532572del , CM000679.1:g.63532561_63532572del GRCh37
NC_000017.9:g.60963023_60963034del NCBI36
NG_012142.1:g.30175_30186del , LRG_296:g.30175_30186del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307078.10:c.2013_2024del MANE Select ENSP00000302625.5:p.Thr672_Arg675del
ENST00000307078.9:c.2013_2024del ENSP00000302625.5:p.Thr672_Arg675del
ENST00000375702.5:c.1818_1829del ENSP00000364854.5:p.Thr607_Arg610del
ENST00000578251.1:n.235_246del
ENST00000611991.1:c.397-7748_397-7737del ENSP00000481191.1:n.397-7748_397-7737del
ENST00000618960.4:c.1818_1829del ENSP00000478916.1:p.Thr607_Arg610del
NM_004655.3:c.2013_2024del , LRG_296t1:c.2013_2024del NP_004646.3:p.Thr672_Arg675del
XM_011525319.1:c.2013_2024del XP_011523621.1:p.Thr672_Arg675del
XM_011525320.1:c.2013_2024del XP_011523622.1:p.Thr672_Arg675del
XM_011525321.1:c.2013_2024del XP_011523623.1:p.Thr672_Arg675del
XM_011525322.1:c.1818_1829del XP_011523624.1:p.Thr607_Arg610del
NM_001363813.1:c.1818_1829del NP_001350742.1:p.Thr607_Arg610del
NM_004655.4:c.2013_2024del MANE Select NP_004646.3:p.Thr672_Arg675del
XM_011525319.2:c.2013_2024del XP_011523621.1:p.Thr672_Arg675del
XM_011525321.2:c.2013_2024del XP_011523623.1:p.Thr672_Arg675del
XM_017025192.1:c.2013_2024del XP_016880681.1:p.Thr672_Arg675del
XM_017025193.1:c.1818_1829del XP_016880682.1:p.Thr607_Arg610del