Canonical Allele Identifier: CA2762343909

Gene: ANTXR2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072707dup , CM000666.2:g.80072707dup	GRCh38
NC_000004.11:g.80993861dup , CM000666.1:g.80993861dup	GRCh37
NC_000004.10:g.81212885dup	NCBI36
NG_015987.1:g.5617dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-147dup MANE Select	ENSP00000385575.2:n.-147dup
ENST00000679571.1:c.-80+2dup	ENSP00000506307.1:n.-80+2dup
ENST00000680913.1:c.-147dup	ENSP00000505640.1:n.-147dup
ENST00000681115.1:c.-147dup	ENSP00000505618.1:n.-147dup
ENST00000681710.1:c.-80+2dup	ENSP00000505865.1:n.-80+2dup
ENST00000403729.6:c.-147dup	ENSP00000385575.2:n.-147dup
ENST00000404191.5:c.-80+688dup	ENSP00000384028.1:n.-80+688dup
ENST00000506286.1:n.630-1053dup
ENST00000514959.1:n.248+6646dup
NM_001145794.1:c.-147dup	NP_001139266.1:n.-147dup
NM_001286780.1:c.-80+688dup	NP_001273709.1:n.-80+688dup
NM_001286781.1:c.-80+2dup	NP_001273710.1:n.-80+2dup
NM_058172.5:c.-147dup	NP_477520.2:n.-147dup
XM_011531587.1:c.-80+688dup	XP_011529889.1:n.-80+688dup
XM_011531587.3:c.-80+688dup	XP_011529889.1:n.-80+688dup
NM_058172.6:c.-147dup MANE Select	NP_477520.2:n.-147dup
NM_001286780.2:c.-80+688dup	NP_001273709.1:n.-80+688dup
NM_001286781.2:c.-80+2dup	NP_001273710.1:n.-80+2dup
NM_001145794.2:c.-147dup	NP_001139266.1:n.-147dup