Canonical Allele Identifier: CA985606132
Gene: AXIN2 HGNC NCBI

Linked Data

dbSNP Id: rs2043925774

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65536649_65536654del , CM000679.2:g.65536649_65536654del GRCh38
NC_000017.10:g.63532767_63532772del , CM000679.1:g.63532767_63532772del GRCh37
NC_000017.9:g.60963229_60963234del NCBI36
NG_012142.1:g.29969_29974del , LRG_296:g.29969_29974del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307078.10:c.1908-101_1908-96del MANE Select ENSP00000302625.5:n.1908-101_1908-96del
ENST00000307078.9:c.1908-101_1908-96del ENSP00000302625.5:n.1908-101_1908-96del
ENST00000375702.5:c.1713-101_1713-96del ENSP00000364854.5:n.1713-101_1713-96del
ENST00000578251.1:n.29_34del
ENST00000611991.1:c.397-7954_397-7949del ENSP00000481191.1:n.397-7954_397-7949del
ENST00000618960.4:c.1713-101_1713-96del ENSP00000478916.1:n.1713-101_1713-96del
NM_004655.3:c.1908-101_1908-96del , LRG_296t1:c.1908-101_1908-96del NP_004646.3:n.1908-101_1908-96del
XM_011525319.1:c.1908-101_1908-96del XP_011523621.1:n.1908-101_1908-96del
XM_011525320.1:c.1908-101_1908-96del XP_011523622.1:n.1908-101_1908-96del
XM_011525321.1:c.1908-101_1908-96del XP_011523623.1:n.1908-101_1908-96del
XM_011525322.1:c.1713-101_1713-96del XP_011523624.1:n.1713-101_1713-96del
NM_001363813.1:c.1713-101_1713-96del NP_001350742.1:n.1713-101_1713-96del
NM_004655.4:c.1908-101_1908-96del MANE Select NP_004646.3:n.1908-101_1908-96del
XM_011525319.2:c.1908-101_1908-96del XP_011523621.1:n.1908-101_1908-96del
XM_011525321.2:c.1908-101_1908-96del XP_011523623.1:n.1908-101_1908-96del
XM_017025192.1:c.1908-101_1908-96del XP_016880681.1:n.1908-101_1908-96del
XM_017025193.1:c.1713-101_1713-96del XP_016880682.1:n.1713-101_1713-96del