Canonical Allele Identifier: CA8719034

Gene: AXIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65558058T>C , CM000679.2:g.65558058T>C	GRCh38
NC_000017.10:g.63554176T>C , CM000679.1:g.63554176T>C	GRCh37
NC_000017.9:g.60984638T>C	NCBI36
NG_012142.1:g.8565A>G , LRG_296:g.8565A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.563A>G MANE Select	ENSP00000302625.5:p.Gln188Arg
ENST00000307078.9:c.563A>G	ENSP00000302625.5:p.Gln188Arg
ENST00000375702.5:c.563A>G	ENSP00000364854.5:p.Gln188Arg
ENST00000577278.1:c.563A>G	ENSP00000464264.1:p.Gln188Arg
ENST00000577662.1:c.878A>G
ENST00000580513.1:c.563A>G	ENSP00000463761.1:p.Gln188Arg
ENST00000585045.1:c.563A>G	ENSP00000463192.1:p.Gln188Arg
ENST00000611991.1:c.396+167A>G	ENSP00000481191.1:n.396+167A>G
ENST00000618960.4:c.563A>G	ENSP00000478916.1:p.Gln188Arg
NM_004655.3:c.563A>G , LRG_296t1:c.563A>G	NP_004646.3:p.Gln188Arg
XM_011525319.1:c.563A>G	XP_011523621.1:p.Gln188Arg
XM_011525320.1:c.563A>G	XP_011523622.1:p.Gln188Arg
XM_011525321.1:c.563A>G	XP_011523623.1:p.Gln188Arg
XM_011525322.1:c.563A>G	XP_011523624.1:p.Gln188Arg
NM_001363813.1:c.563A>G	NP_001350742.1:p.Gln188Arg
NM_004655.4:c.563A>G MANE Select	NP_004646.3:p.Gln188Arg
XM_011525319.2:c.563A>G	XP_011523621.1:p.Gln188Arg
XM_011525321.2:c.563A>G	XP_011523623.1:p.Gln188Arg
XM_017025192.1:c.563A>G	XP_016880681.1:p.Gln188Arg
XM_017025193.1:c.563A>G	XP_016880682.1:p.Gln188Arg