Canonical Allele Identifier: CA2270883534
Gene: AXIN2 HGNC NCBI

Linked Data

dbSNP Id: rs2043925504

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65536642_65536643del , CM000679.2:g.65536642_65536643del GRCh38
NC_000017.10:g.63532760_63532761del , CM000679.1:g.63532760_63532761del GRCh37
NC_000017.9:g.60963222_60963223del NCBI36
NG_012142.1:g.29980_29981del , LRG_296:g.29980_29981del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307078.10:c.1908-90_1908-89del MANE Select ENSP00000302625.5:n.1908-90_1908-89del
ENST00000307078.9:c.1908-90_1908-89del ENSP00000302625.5:n.1908-90_1908-89del
ENST00000375702.5:c.1713-90_1713-89del ENSP00000364854.5:n.1713-90_1713-89del
ENST00000578251.1:n.40_41del
ENST00000611991.1:c.397-7943_397-7942del ENSP00000481191.1:n.397-7943_397-7942del
ENST00000618960.4:c.1713-90_1713-89del ENSP00000478916.1:n.1713-90_1713-89del
NM_004655.3:c.1908-90_1908-89del , LRG_296t1:c.1908-90_1908-89del NP_004646.3:n.1908-90_1908-89del
XM_011525319.1:c.1908-90_1908-89del XP_011523621.1:n.1908-90_1908-89del
XM_011525320.1:c.1908-90_1908-89del XP_011523622.1:n.1908-90_1908-89del
XM_011525321.1:c.1908-90_1908-89del XP_011523623.1:n.1908-90_1908-89del
XM_011525322.1:c.1713-90_1713-89del XP_011523624.1:n.1713-90_1713-89del
NM_001363813.1:c.1713-90_1713-89del NP_001350742.1:n.1713-90_1713-89del
NM_004655.4:c.1908-90_1908-89del MANE Select NP_004646.3:n.1908-90_1908-89del
XM_011525319.2:c.1908-90_1908-89del XP_011523621.1:n.1908-90_1908-89del
XM_011525321.2:c.1908-90_1908-89del XP_011523623.1:n.1908-90_1908-89del
XM_017025192.1:c.1908-90_1908-89del XP_016880681.1:n.1908-90_1908-89del
XM_017025193.1:c.1713-90_1713-89del XP_016880682.1:n.1713-90_1713-89del