Canonical Allele Identifier: CA1471242752

Gene: ANTXR2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072750_80072751delinsAG , CM000666.2:g.80072750_80072751delinsAG	GRCh38
NC_000004.11:g.80993904_80993905delinsAG , CM000666.1:g.80993904_80993905delinsAG	GRCh37
NC_000004.10:g.81212928_81212929delinsAG	NCBI36
NG_015987.1:g.5573_5574delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-191_-190delinsCT MANE Select	ENSP00000385575.2:n.-191_-190delinsCT
ENST00000679571.1:c.-122_-121delinsCT	ENSP00000506307.1:n.-122_-121delinsCT
ENST00000681115.1:c.-191_-190delinsCT	ENSP00000505618.1:n.-191_-190delinsCT
ENST00000681710.1:c.-122_-121delinsCT	ENSP00000505865.1:n.-122_-121delinsCT
ENST00000403729.6:c.-191_-190delinsCT	ENSP00000385575.2:n.-191_-190delinsCT
ENST00000404191.5:c.-80+644_-80+645delinsCT	ENSP00000384028.1:n.-80+644_-80+645delinsCT
ENST00000506286.1:n.630-1097_630-1096delinsCT
ENST00000514959.1:n.248+6602_248+6603delinsCT
NM_001145794.1:c.-191_-190delinsCT	NP_001139266.1:n.-191_-190delinsCT
NM_001286780.1:c.-80+644_-80+645delinsCT	NP_001273709.1:n.-80+644_-80+645delinsCT
NM_001286781.1:c.-122_-121delinsCT	NP_001273710.1:n.-122_-121delinsCT
NM_058172.5:c.-191_-190delinsCT	NP_477520.2:n.-191_-190delinsCT
XM_011531587.1:c.-80+644_-80+645delinsCT	XP_011529889.1:n.-80+644_-80+645delinsCT
XM_011531587.3:c.-80+644_-80+645delinsCT	XP_011529889.1:n.-80+644_-80+645delinsCT
NM_058172.6:c.-191_-190delinsCT MANE Select	NP_477520.2:n.-191_-190delinsCT
NM_001286780.2:c.-80+644_-80+645delinsCT	NP_001273709.1:n.-80+644_-80+645delinsCT
NM_001286781.2:c.-122_-121delinsCT	NP_001273710.1:n.-122_-121delinsCT
NM_001145794.2:c.-191_-190delinsCT	NP_001139266.1:n.-191_-190delinsCT