Canonical Allele Identifier: CA2580094673

Gene: AXIN2

Linked Data

• ClinVar Variation Id: 2039954
• ClinVar RCV Id: RCV002886149

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536527_65536533del , CM000679.2:g.65536527_65536533del	GRCh38
NC_000017.10:g.63532645_63532651del , CM000679.1:g.63532645_63532651del	GRCh37
NC_000017.9:g.60963107_60963113del	NCBI36
NG_012142.1:g.30091_30097del , LRG_296:g.30091_30097del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.1929_1935del MANE Select	ENSP00000302625.5:p.Tyr644TrpfsTer?
ENST00000307078.9:c.1929_1935del	ENSP00000302625.5:p.Tyr644TrpfsTer?
ENST00000375702.5:c.1734_1740del	ENSP00000364854.5:p.Tyr579TrpfsTer?
ENST00000578251.1:n.151_157del
ENST00000611991.1:c.397-7832_397-7826del	ENSP00000481191.1:n.397-7832_397-7826del
ENST00000618960.4:c.1734_1740del	ENSP00000478916.1:p.Tyr579TrpfsTer?
NM_004655.3:c.1929_1935del , LRG_296t1:c.1929_1935del	NP_004646.3:p.Tyr644TrpfsTer?
XM_011525319.1:c.1929_1935del	XP_011523621.1:p.Tyr644TrpfsTer?
XM_011525320.1:c.1929_1935del	XP_011523622.1:p.Tyr644TrpfsTer?
XM_011525321.1:c.1929_1935del	XP_011523623.1:p.Tyr644TrpfsTer?
XM_011525322.1:c.1734_1740del	XP_011523624.1:p.Tyr579TrpfsTer?
NM_001363813.1:c.1734_1740del	NP_001350742.1:p.Tyr579TrpfsTer?
NM_004655.4:c.1929_1935del MANE Select	NP_004646.3:p.Tyr644TrpfsTer?
XM_011525319.2:c.1929_1935del	XP_011523621.1:p.Tyr644TrpfsTer?
XM_011525321.2:c.1929_1935del	XP_011523623.1:p.Tyr644TrpfsTer?
XM_017025192.1:c.1929_1935del	XP_016880681.1:p.Tyr644TrpfsTer?
XM_017025193.1:c.1734_1740del	XP_016880682.1:p.Tyr579TrpfsTer?