Canonical Allele Identifier: CA1471242051

Gene: ANTXR2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072458C= , CM000666.2:g.80072458C=	GRCh38
NC_000004.11:g.80993612C= , CM000666.1:g.80993612C=	GRCh37
NC_000004.10:g.81212636C=	NCBI36
NG_015987.1:g.5866G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.103G= MANE Select	ENSP00000385575.2:p.Glu35=
ENST00000679571.1:c.-80+251G=	ENSP00000506307.1:n.-80+251G=
ENST00000680913.1:c.103G=	ENSP00000505640.1:p.Glu35=
ENST00000681115.1:c.103G=	ENSP00000505618.1:p.Glu35=
ENST00000681710.1:c.-80+251G=	ENSP00000505865.1:n.-80+251G=
ENST00000307333.7:c.103G=	ENSP00000306185.6:p.Glu35=
ENST00000346652.10:c.103G=	ENSP00000314883.6:p.Glu35=
ENST00000403729.6:c.103G=	ENSP00000385575.2:p.Glu35=
ENST00000404191.5:c.-79-804G=	ENSP00000384028.1:n.-79-804G=
ENST00000506286.1:n.630-804G=
ENST00000514959.1:n.248+6895G=
NM_001145794.1:c.103G=	NP_001139266.1:p.Glu35=
NM_001286780.1:c.-79-804G=	NP_001273709.1:n.-79-804G=
NM_001286781.1:c.-80+251G=	NP_001273710.1:n.-80+251G=
NM_058172.5:c.103G=	NP_477520.2:p.Glu35=
XM_011531587.1:c.-79-804G=	XP_011529889.1:n.-79-804G=
XM_011531587.3:c.-79-804G=	XP_011529889.1:n.-79-804G=
NM_058172.6:c.103G= MANE Select	NP_477520.2:p.Glu35=
NM_001286780.2:c.-79-804G=	NP_001273709.1:n.-79-804G=
NM_001286781.2:c.-80+251G=	NP_001273710.1:n.-80+251G=
NM_001145794.2:c.103G=	NP_001139266.1:p.Glu35=