Canonical Allele Identifier: CA2639404761
Gene: AXIN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65536669_65536671dup , CM000679.2:g.65536669_65536671dup GRCh38
NC_000017.10:g.63532787_63532789dup , CM000679.1:g.63532787_63532789dup GRCh37
NC_000017.9:g.60963249_60963251dup NCBI36
NG_012142.1:g.29959_29961dup , LRG_296:g.29959_29961dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307078.10:c.1908-111_1908-109dup MANE Select ENSP00000302625.5:n.1908-111_1908-109dup
ENST00000307078.9:c.1908-111_1908-109dup ENSP00000302625.5:n.1908-111_1908-109dup
ENST00000375702.5:c.1713-111_1713-109dup ENSP00000364854.5:n.1713-111_1713-109dup
ENST00000578251.1:n.19_21dup
ENST00000611991.1:c.397-7964_397-7962dup ENSP00000481191.1:n.397-7964_397-7962dup
ENST00000618960.4:c.1713-111_1713-109dup ENSP00000478916.1:n.1713-111_1713-109dup
NM_004655.3:c.1908-111_1908-109dup , LRG_296t1:c.1908-111_1908-109dup NP_004646.3:n.1908-111_1908-109dup
XM_011525319.1:c.1908-111_1908-109dup XP_011523621.1:n.1908-111_1908-109dup
XM_011525320.1:c.1908-111_1908-109dup XP_011523622.1:n.1908-111_1908-109dup
XM_011525321.1:c.1908-111_1908-109dup XP_011523623.1:n.1908-111_1908-109dup
XM_011525322.1:c.1713-111_1713-109dup XP_011523624.1:n.1713-111_1713-109dup
NM_001363813.1:c.1713-111_1713-109dup NP_001350742.1:n.1713-111_1713-109dup
NM_004655.4:c.1908-111_1908-109dup MANE Select NP_004646.3:n.1908-111_1908-109dup
XM_011525319.2:c.1908-111_1908-109dup XP_011523621.1:n.1908-111_1908-109dup
XM_011525321.2:c.1908-111_1908-109dup XP_011523623.1:n.1908-111_1908-109dup
XM_017025192.1:c.1908-111_1908-109dup XP_016880681.1:n.1908-111_1908-109dup
XM_017025193.1:c.1713-111_1713-109dup XP_016880682.1:n.1713-111_1713-109dup