Canonical Allele Identifier: CA501690969

Gene: AXIN2

Linked Data

• MyVariant Identifiers: chr17:g.63532585_63532586insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536467_65536468insG , CM000679.2:g.65536467_65536468insG	GRCh38
NC_000017.10:g.63532585_63532586insG , CM000679.1:g.63532585_63532586insG	GRCh37
NC_000017.9:g.60963047_60963048insG	NCBI36
NG_012142.1:g.30155_30156insC , LRG_296:g.30155_30156insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.1993_1994insC MANE Select	ENSP00000302625.5:p.Gly665AlafsTer?
ENST00000307078.9:c.1993_1994insC	ENSP00000302625.5:p.Gly665AlafsTer?
ENST00000375702.5:c.1798_1799insC	ENSP00000364854.5:p.Gly600AlafsTer?
ENST00000578251.1:n.215_216insC
ENST00000611991.1:c.397-7768_397-7767insC	ENSP00000481191.1:n.397-7768_397-7767insC
ENST00000618960.4:c.1798_1799insC	ENSP00000478916.1:p.Gly600AlafsTer?
NM_004655.3:c.1993_1994insC , LRG_296t1:c.1993_1994insC	NP_004646.3:p.Gly665AlafsTer?
XM_011525319.1:c.1993_1994insC	XP_011523621.1:p.Gly665AlafsTer?
XM_011525320.1:c.1993_1994insC	XP_011523622.1:p.Gly665AlafsTer?
XM_011525321.1:c.1993_1994insC	XP_011523623.1:p.Gly665AlafsTer?
XM_011525322.1:c.1798_1799insC	XP_011523624.1:p.Gly600AlafsTer?
NM_001363813.1:c.1798_1799insC	NP_001350742.1:p.Gly600AlafsTer?
NM_004655.4:c.1993_1994insC MANE Select	NP_004646.3:p.Gly665AlafsTer?
XM_011525319.2:c.1993_1994insC	XP_011523621.1:p.Gly665AlafsTer?
XM_011525321.2:c.1993_1994insC	XP_011523623.1:p.Gly665AlafsTer?
XM_017025192.1:c.1993_1994insC	XP_016880681.1:p.Gly665AlafsTer?
XM_017025193.1:c.1798_1799insC	XP_016880682.1:p.Gly600AlafsTer?