Canonical Allele Identifier: CA916081919

Gene: AXIN2

Linked Data

• ClinVar Variation Id: 835332
• ClinVar RCV Id: RCV001036188
• dbSNP Id: rs2043922406

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536563_65536564delinsTT , CM000679.2:g.65536563_65536564delinsTT	GRCh38
NC_000017.10:g.63532681_63532682delinsTT , CM000679.1:g.63532681_63532682delinsTT	GRCh37
NC_000017.9:g.60963143_60963144delinsTT	NCBI36
NG_012142.1:g.30059_30060delinsAA , LRG_296:g.30059_30060delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.1908-11_1908-10delinsAA MANE Select	ENSP00000302625.5:n.1908-11_1908-10delinsAA
ENST00000307078.9:c.1908-11_1908-10delinsAA	ENSP00000302625.5:n.1908-11_1908-10delinsAA
ENST00000375702.5:c.1713-11_1713-10delinsAA	ENSP00000364854.5:n.1713-11_1713-10delinsAA
ENST00000578251.1:n.119_120delinsAA
ENST00000611991.1:c.397-7864_397-7863delinsAA	ENSP00000481191.1:n.397-7864_397-7863delinsAA
ENST00000618960.4:c.1713-11_1713-10delinsAA	ENSP00000478916.1:n.1713-11_1713-10delinsAA
NM_004655.3:c.1908-11_1908-10delinsAA , LRG_296t1:c.1908-11_1908-10delinsAA	NP_004646.3:n.1908-11_1908-10delinsAA
XM_011525319.1:c.1908-11_1908-10delinsAA	XP_011523621.1:n.1908-11_1908-10delinsAA
XM_011525320.1:c.1908-11_1908-10delinsAA	XP_011523622.1:n.1908-11_1908-10delinsAA
XM_011525321.1:c.1908-11_1908-10delinsAA	XP_011523623.1:n.1908-11_1908-10delinsAA
XM_011525322.1:c.1713-11_1713-10delinsAA	XP_011523624.1:n.1713-11_1713-10delinsAA
NM_001363813.1:c.1713-11_1713-10delinsAA	NP_001350742.1:n.1713-11_1713-10delinsAA
NM_004655.4:c.1908-11_1908-10delinsAA MANE Select	NP_004646.3:n.1908-11_1908-10delinsAA
XM_011525319.2:c.1908-11_1908-10delinsAA	XP_011523621.1:n.1908-11_1908-10delinsAA
XM_011525321.2:c.1908-11_1908-10delinsAA	XP_011523623.1:n.1908-11_1908-10delinsAA
XM_017025192.1:c.1908-11_1908-10delinsAA	XP_016880681.1:n.1908-11_1908-10delinsAA
XM_017025193.1:c.1713-11_1713-10delinsAA	XP_016880682.1:n.1713-11_1713-10delinsAA