Canonical Allele Identifier: CA293097891

Gene: AXIN2

Linked Data

• dbSNP Id: rs772221486
• gnomAD v2: 17-63532766-TCA-T
• gnomAD v3: 17-65536648-TCA-T
• gnomAD v4: 17-65536648-TCA-T
• MyVariant Identifiers: chr17:g.63532767_63532768del (hg19) ; chr17:g.65536649_65536650del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.65536649_65536650del , CM000679.2:g.65536649_65536650del	GRCh38
NC_000017.10:g.63532767_63532768del , CM000679.1:g.63532767_63532768del	GRCh37
NC_000017.9:g.60963229_60963230del	NCBI36
NG_012142.1:g.29973_29974del , LRG_296:g.29973_29974del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307078.10:c.1908-97_1908-96del MANE Select	ENSP00000302625.5:n.1908-97_1908-96del
ENST00000307078.9:c.1908-97_1908-96del	ENSP00000302625.5:n.1908-97_1908-96del
ENST00000375702.5:c.1713-97_1713-96del	ENSP00000364854.5:n.1713-97_1713-96del
ENST00000578251.1:n.33_34del
ENST00000611991.1:c.397-7950_397-7949del	ENSP00000481191.1:n.397-7950_397-7949del
ENST00000618960.4:c.1713-97_1713-96del	ENSP00000478916.1:n.1713-97_1713-96del
NM_004655.3:c.1908-97_1908-96del , LRG_296t1:c.1908-97_1908-96del	NP_004646.3:n.1908-97_1908-96del
XM_011525319.1:c.1908-97_1908-96del	XP_011523621.1:n.1908-97_1908-96del
XM_011525320.1:c.1908-97_1908-96del	XP_011523622.1:n.1908-97_1908-96del
XM_011525321.1:c.1908-97_1908-96del	XP_011523623.1:n.1908-97_1908-96del
XM_011525322.1:c.1713-97_1713-96del	XP_011523624.1:n.1713-97_1713-96del
NM_001363813.1:c.1713-97_1713-96del	NP_001350742.1:n.1713-97_1713-96del
NM_004655.4:c.1908-97_1908-96del MANE Select	NP_004646.3:n.1908-97_1908-96del
XM_011525319.2:c.1908-97_1908-96del	XP_011523621.1:n.1908-97_1908-96del
XM_011525321.2:c.1908-97_1908-96del	XP_011523623.1:n.1908-97_1908-96del
XM_017025192.1:c.1908-97_1908-96del	XP_016880681.1:n.1908-97_1908-96del
XM_017025193.1:c.1713-97_1713-96del	XP_016880682.1:n.1713-97_1713-96del