Canonical Allele Identifier: CA649318562

Gene: ANTXR2

Linked Data

• COSMIC: COSN22302011

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072694_80072695insC , CM000666.2:g.80072694_80072695insC	GRCh38
NC_000004.11:g.80993848_80993849insC , CM000666.1:g.80993848_80993849insC	GRCh37
NC_000004.10:g.81212872_81212873insC	NCBI36
NG_015987.1:g.5629_5630insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-135_-134insG MANE Select	ENSP00000385575.2:n.-135_-134insG
ENST00000679571.1:c.-80+14_-80+15insG	ENSP00000506307.1:n.-80+14_-80+15insG
ENST00000680913.1:c.-135_-134insG	ENSP00000505640.1:n.-135_-134insG
ENST00000681115.1:c.-135_-134insG	ENSP00000505618.1:n.-135_-134insG
ENST00000681710.1:c.-80+14_-80+15insG	ENSP00000505865.1:n.-80+14_-80+15insG
ENST00000346652.10:c.-135_-134insG	ENSP00000314883.6:n.-135_-134insG
ENST00000403729.6:c.-135_-134insG	ENSP00000385575.2:n.-135_-134insG
ENST00000404191.5:c.-80+700_-80+701insG	ENSP00000384028.1:n.-80+700_-80+701insG
ENST00000506286.1:n.630-1041_630-1040insG
ENST00000514959.1:n.248+6658_248+6659insG
NM_001145794.1:c.-135_-134insG	NP_001139266.1:n.-135_-134insG
NM_001286780.1:c.-80+700_-80+701insG	NP_001273709.1:n.-80+700_-80+701insG
NM_001286781.1:c.-80+14_-80+15insG	NP_001273710.1:n.-80+14_-80+15insG
NM_058172.5:c.-135_-134insG	NP_477520.2:n.-135_-134insG
XM_011531587.1:c.-80+700_-80+701insG	XP_011529889.1:n.-80+700_-80+701insG
XM_011531587.3:c.-80+700_-80+701insG	XP_011529889.1:n.-80+700_-80+701insG
NM_058172.6:c.-135_-134insG MANE Select	NP_477520.2:n.-135_-134insG
NM_001286780.2:c.-80+700_-80+701insG	NP_001273709.1:n.-80+700_-80+701insG
NM_001286781.2:c.-80+14_-80+15insG	NP_001273710.1:n.-80+14_-80+15insG
NM_001145794.2:c.-135_-134insG	NP_001139266.1:n.-135_-134insG