Canonical Allele Identifier: CA891844415

Gene: AXIN2

Linked Data

• ClinVar Variation Id: 579998
• ClinVar RCV Id: RCV000703417

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536447_65536448delinsCA , CM000679.2:g.65536447_65536448delinsCA	GRCh38
NC_000017.10:g.63532565_63532566delinsCA , CM000679.1:g.63532565_63532566delinsCA	GRCh37
NC_000017.9:g.60963027_60963028delinsCA	NCBI36
NG_012142.1:g.30175_30176delinsTG , LRG_296:g.30175_30176delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.2013_2014delinsTG MANE Select	ENSP00000302625.5:p.Thr672Ala
ENST00000307078.9:c.2013_2014delinsTG	ENSP00000302625.5:p.Thr672Ala
ENST00000375702.5:c.1818_1819delinsTG	ENSP00000364854.5:p.Thr607Ala
ENST00000578251.1:n.235_236delinsTG
ENST00000611991.1:c.397-7748_397-7747delinsTG	ENSP00000481191.1:n.397-7748_397-7747delinsTG
ENST00000618960.4:c.1818_1819delinsTG	ENSP00000478916.1:p.Thr607Ala
NM_004655.3:c.2013_2014delinsTG , LRG_296t1:c.2013_2014delinsTG	NP_004646.3:p.Thr672Ala
XM_011525319.1:c.2013_2014delinsTG	XP_011523621.1:p.Thr672Ala
XM_011525320.1:c.2013_2014delinsTG	XP_011523622.1:p.Thr672Ala
XM_011525321.1:c.2013_2014delinsTG	XP_011523623.1:p.Thr672Ala
XM_011525322.1:c.1818_1819delinsTG	XP_011523624.1:p.Thr607Ala
NM_001363813.1:c.1818_1819delinsTG	NP_001350742.1:p.Thr607Ala
NM_004655.4:c.2013_2014delinsTG MANE Select	NP_004646.3:p.Thr672Ala
XM_011525319.2:c.2013_2014delinsTG	XP_011523621.1:p.Thr672Ala
XM_011525321.2:c.2013_2014delinsTG	XP_011523623.1:p.Thr672Ala
XM_017025192.1:c.2013_2014delinsTG	XP_016880681.1:p.Thr672Ala
XM_017025193.1:c.1818_1819delinsTG	XP_016880682.1:p.Thr607Ala