Canonical Allele Identifier: CA2270883574

Gene: AXIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536688_65536689delinsAG , CM000679.2:g.65536688_65536689delinsAG	GRCh38
NC_000017.10:g.63532806_63532807delinsAG , CM000679.1:g.63532806_63532807delinsAG	GRCh37
NC_000017.9:g.60963268_60963269delinsAG	NCBI36
NG_012142.1:g.29934_29935delinsCT , LRG_296:g.29934_29935delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.1908-136_1908-135delinsCT MANE Select	ENSP00000302625.5:n.1908-136_1908-135delinsCT
ENST00000307078.9:c.1908-136_1908-135delinsCT	ENSP00000302625.5:n.1908-136_1908-135delinsCT
ENST00000375702.5:c.1713-136_1713-135delinsCT	ENSP00000364854.5:n.1713-136_1713-135delinsCT
ENST00000611991.1:c.397-7989_397-7988delinsCT	ENSP00000481191.1:n.397-7989_397-7988delinsCT
ENST00000618960.4:c.1713-136_1713-135delinsCT	ENSP00000478916.1:n.1713-136_1713-135delinsCT
NM_004655.3:c.1908-136_1908-135delinsCT , LRG_296t1:c.1908-136_1908-135delinsCT	NP_004646.3:n.1908-136_1908-135delinsCT
XM_011525319.1:c.1908-136_1908-135delinsCT	XP_011523621.1:n.1908-136_1908-135delinsCT
XM_011525320.1:c.1908-136_1908-135delinsCT	XP_011523622.1:n.1908-136_1908-135delinsCT
XM_011525321.1:c.1908-136_1908-135delinsCT	XP_011523623.1:n.1908-136_1908-135delinsCT
XM_011525322.1:c.1713-136_1713-135delinsCT	XP_011523624.1:n.1713-136_1713-135delinsCT
NM_001363813.1:c.1713-136_1713-135delinsCT	NP_001350742.1:n.1713-136_1713-135delinsCT
NM_004655.4:c.1908-136_1908-135delinsCT MANE Select	NP_004646.3:n.1908-136_1908-135delinsCT
XM_011525319.2:c.1908-136_1908-135delinsCT	XP_011523621.1:n.1908-136_1908-135delinsCT
XM_011525321.2:c.1908-136_1908-135delinsCT	XP_011523623.1:n.1908-136_1908-135delinsCT
XM_017025192.1:c.1908-136_1908-135delinsCT	XP_016880681.1:n.1908-136_1908-135delinsCT
XM_017025193.1:c.1713-136_1713-135delinsCT	XP_016880682.1:n.1713-136_1713-135delinsCT