Canonical Allele Identifier: CA2576361295

Gene: AXIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536431_65536434del , CM000679.2:g.65536431_65536434del	GRCh38
NC_000017.10:g.63532549_63532552del , CM000679.1:g.63532549_63532552del	GRCh37
NC_000017.9:g.60963011_60963014del	NCBI36
NG_012142.1:g.30191_30194del , LRG_296:g.30191_30194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.2029_2032del MANE Select	ENSP00000302625.5:p.His677CysfsTer11
ENST00000307078.9:c.2029_2032del	ENSP00000302625.5:p.His677CysfsTer11
ENST00000375702.5:c.1834_1837del	ENSP00000364854.5:p.His612CysfsTer11
ENST00000578251.1:n.251_254del
ENST00000611991.1:c.397-7732_397-7729del	ENSP00000481191.1:n.397-7732_397-7729del
ENST00000618960.4:c.1834_1837del	ENSP00000478916.1:p.His612CysfsTer11
NM_004655.3:c.2029_2032del , LRG_296t1:c.2029_2032del	NP_004646.3:p.His677CysfsTer11
XM_011525319.1:c.2029_2032del	XP_011523621.1:p.His677CysfsTer11
XM_011525320.1:c.2029_2032del	XP_011523622.1:p.His677CysfsTer11
XM_011525321.1:c.2029_2032del	XP_011523623.1:p.His677CysfsTer11
XM_011525322.1:c.1834_1837del	XP_011523624.1:p.His612CysfsTer11
NM_001363813.1:c.1834_1837del	NP_001350742.1:p.His612CysfsTer11
NM_004655.4:c.2029_2032del MANE Select	NP_004646.3:p.His677CysfsTer11
XM_011525319.2:c.2029_2032del	XP_011523621.1:p.His677CysfsTer11
XM_011525321.2:c.2029_2032del	XP_011523623.1:p.His677CysfsTer11
XM_017025192.1:c.2029_2032del	XP_016880681.1:p.His677CysfsTer11
XM_017025193.1:c.1834_1837del	XP_016880682.1:p.His612CysfsTer11