Canonical Allele Identifier: CA298425
Gene: AXIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182022
dbSNP Id: rs730881405

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.65536527G>A , CM000679.2:g.65536527G>A GRCh38
NC_000017.10:g.63532645G>A , CM000679.1:g.63532645G>A GRCh37
NC_000017.9:g.60963107G>A NCBI36
NG_012142.1:g.30096C>T , LRG_296:g.30096C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307078.10:c.1934C>T MANE Select ENSP00000302625.5:p.Pro645Leu
ENST00000307078.9:c.1934C>T ENSP00000302625.5:p.Pro645Leu
ENST00000375702.5:c.1739C>T ENSP00000364854.5:p.Pro580Leu
ENST00000578251.1:n.156C>T
ENST00000611991.1:c.397-7827C>T ENSP00000481191.1:n.397-7827C>T
ENST00000618960.4:c.1739C>T ENSP00000478916.1:p.Pro580Leu
NM_004655.3:c.1934C>T , LRG_296t1:c.1934C>T NP_004646.3:p.Pro645Leu
XM_011525319.1:c.1934C>T XP_011523621.1:p.Pro645Leu
XM_011525320.1:c.1934C>T XP_011523622.1:p.Pro645Leu
XM_011525321.1:c.1934C>T XP_011523623.1:p.Pro645Leu
XM_011525322.1:c.1739C>T XP_011523624.1:p.Pro580Leu
NM_001363813.1:c.1739C>T NP_001350742.1:p.Pro580Leu
NM_004655.4:c.1934C>T MANE Select NP_004646.3:p.Pro645Leu
XM_011525319.2:c.1934C>T XP_011523621.1:p.Pro645Leu
XM_011525321.2:c.1934C>T XP_011523623.1:p.Pro645Leu
XM_017025192.1:c.1934C>T XP_016880681.1:p.Pro645Leu
XM_017025193.1:c.1739C>T XP_016880682.1:p.Pro580Leu