Canonical Allele Identifier: CA2573154710

Gene: AXIN2

Linked Data

• ClinVar Variation Id: 1378845
• ClinVar RCV Id: RCV001891838
• dbSNP Id: rs2144441207

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536423_65536424del , CM000679.2:g.65536423_65536424del	GRCh38
NC_000017.10:g.63532541_63532542del , CM000679.1:g.63532541_63532542del	GRCh37
NC_000017.9:g.60963003_60963004del	NCBI36
NG_012142.1:g.30200_30201del , LRG_296:g.30200_30201del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.2038_2039del MANE Select	ENSP00000302625.5:p.Thr680ProfsTer26
ENST00000307078.9:c.2038_2039del	ENSP00000302625.5:p.Thr680ProfsTer26
ENST00000375702.5:c.1843_1844del	ENSP00000364854.5:p.Thr615ProfsTer26
ENST00000578251.1:n.260_261del
ENST00000611991.1:c.397-7723_397-7722del	ENSP00000481191.1:n.397-7723_397-7722del
ENST00000618960.4:c.1843_1844del	ENSP00000478916.1:p.Thr615ProfsTer26
NM_004655.3:c.2038_2039del , LRG_296t1:c.2038_2039del	NP_004646.3:p.Thr680ProfsTer26
XM_011525319.1:c.2038_2039del	XP_011523621.1:p.Thr680ProfsTer26
XM_011525320.1:c.2038_2039del	XP_011523622.1:p.Thr680ProfsTer26
XM_011525321.1:c.2038_2039del	XP_011523623.1:p.Thr680ProfsTer26
XM_011525322.1:c.1843_1844del	XP_011523624.1:p.Thr615ProfsTer26
NM_001363813.1:c.1843_1844del	NP_001350742.1:p.Thr615ProfsTer26
NM_004655.4:c.2038_2039del MANE Select	NP_004646.3:p.Thr680ProfsTer26
XM_011525319.2:c.2038_2039del	XP_011523621.1:p.Thr680ProfsTer26
XM_011525321.2:c.2038_2039del	XP_011523623.1:p.Thr680ProfsTer26
XM_017025192.1:c.2038_2039del	XP_016880681.1:p.Thr680ProfsTer26
XM_017025193.1:c.1843_1844del	XP_016880682.1:p.Thr615ProfsTer26