Canonical Allele Identifier: CA1471242770

Gene: ANTXR2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072764_80072776delinsACCGCCGCAGCTG , CM000666.2:g.80072764_80072776delinsACCGCCGCAGCTG	GRCh38
NC_000004.11:g.80993918_80993930delinsACCGCCGCAGCTG , CM000666.1:g.80993918_80993930delinsACCGCCGCAGCTG	GRCh37
NC_000004.10:g.81212942_81212954delinsACCGCCGCAGCTG	NCBI36
NG_015987.1:g.5548_5560delinsCAGCTGCGGCGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-216_-204delinsCAGCTGCGGCGGT MANE Select	ENSP00000385575.2:n.-216_-204delinsCAGCTGCGGCGGT
ENST00000679571.1:c.-147_-135delinsCAGCTGCGGCGGT	ENSP00000506307.1:n.-147_-135delinsCAGCTGCGGCGGT
ENST00000681115.1:c.-216_-204delinsCAGCTGCGGCGGT	ENSP00000505618.1:n.-216_-204delinsCAGCTGCGGCGGT
ENST00000681710.1:c.-147_-135delinsCAGCTGCGGCGGT	ENSP00000505865.1:n.-147_-135delinsCAGCTGCGGCGGT
ENST00000403729.6:c.-216_-204delinsCAGCTGCGGCGGT	ENSP00000385575.2:n.-216_-204delinsCAGCTGCGGCGGT
ENST00000404191.5:c.-80+619_-80+631delinsCAGCTGCGGCGGT	ENSP00000384028.1:n.-80+619_-80+631delinsCAGCTGCGGCGGT
ENST00000506286.1:n.630-1122_630-1110delinsCAGCTGCGGCGGT
ENST00000514959.1:n.248+6577_248+6589delinsCAGCTGCGGCGGT
NM_001145794.1:c.-216_-204delinsCAGCTGCGGCGGT	NP_001139266.1:n.-216_-204delinsCAGCTGCGGCGGT
NM_001286780.1:c.-80+619_-80+631delinsCAGCTGCGGCGGT	NP_001273709.1:n.-80+619_-80+631delinsCAGCTGCGGCGGT
NM_001286781.1:c.-147_-135delinsCAGCTGCGGCGGT	NP_001273710.1:n.-147_-135delinsCAGCTGCGGCGGT
NM_058172.5:c.-216_-204delinsCAGCTGCGGCGGT	NP_477520.2:n.-216_-204delinsCAGCTGCGGCGGT
XM_011531587.1:c.-80+619_-80+631delinsCAGCTGCGGCGGT	XP_011529889.1:n.-80+619_-80+631delinsCAGCTGCGGCGGT
XM_011531587.3:c.-80+619_-80+631delinsCAGCTGCGGCGGT	XP_011529889.1:n.-80+619_-80+631delinsCAGCTGCGGCGGT
NM_058172.6:c.-216_-204delinsCAGCTGCGGCGGT MANE Select	NP_477520.2:n.-216_-204delinsCAGCTGCGGCGGT
NM_001286780.2:c.-80+619_-80+631delinsCAGCTGCGGCGGT	NP_001273709.1:n.-80+619_-80+631delinsCAGCTGCGGCGGT
NM_001286781.2:c.-147_-135delinsCAGCTGCGGCGGT	NP_001273710.1:n.-147_-135delinsCAGCTGCGGCGGT
NM_001145794.2:c.-216_-204delinsCAGCTGCGGCGGT	NP_001139266.1:n.-216_-204delinsCAGCTGCGGCGGT