Canonical Allele Identifier: CA400682490

Gene: AXIN2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65558607A>G , CM000679.2:g.65558607A>G	GRCh38
NC_000017.10:g.63554725A>G , CM000679.1:g.63554725A>G	GRCh37
NC_000017.9:g.60985187A>G	NCBI36
NG_012142.1:g.8016T>C , LRG_296:g.8016T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.14T>C MANE Select	ENSP00000302625.5:p.Met5Thr
ENST00000307078.9:c.14T>C	ENSP00000302625.5:p.Met5Thr
ENST00000375702.5:c.14T>C	ENSP00000364854.5:p.Met5Thr
ENST00000544103.2:c.14T>C	ENSP00000441151.2:p.Met5Thr
ENST00000577278.1:c.14T>C	ENSP00000464264.1:p.Met5Thr
ENST00000577662.1:c.329T>C
ENST00000580513.1:c.14T>C	ENSP00000463761.1:p.Met5Thr
ENST00000585045.1:c.14T>C	ENSP00000463192.1:p.Met5Thr
ENST00000611991.1:c.14T>C	ENSP00000481191.1:p.Met5Thr
ENST00000618960.4:c.14T>C	ENSP00000478916.1:p.Met5Thr
NM_004655.3:c.14T>C , LRG_296t1:c.14T>C	NP_004646.3:p.Met5Thr
XM_011525319.1:c.14T>C	XP_011523621.1:p.Met5Thr
XM_011525320.1:c.14T>C	XP_011523622.1:p.Met5Thr
XM_011525321.1:c.14T>C	XP_011523623.1:p.Met5Thr
XM_011525322.1:c.14T>C	XP_011523624.1:p.Met5Thr
NM_001363813.1:c.14T>C	NP_001350742.1:p.Met5Thr
NM_004655.4:c.14T>C MANE Select	NP_004646.3:p.Met5Thr
XM_011525319.2:c.14T>C	XP_011523621.1:p.Met5Thr
XM_011525321.2:c.14T>C	XP_011523623.1:p.Met5Thr
XM_017025192.1:c.14T>C	XP_016880681.1:p.Met5Thr
XM_017025193.1:c.14T>C	XP_016880682.1:p.Met5Thr