Canonical Allele Identifier: CA1471242714

Gene: ANTXR2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.80072728G= , CM000666.2:g.80072728G=	GRCh38
NC_000004.11:g.80993882G= , CM000666.1:g.80993882G=	GRCh37
NC_000004.10:g.81212906G=	NCBI36
NG_015987.1:g.5596C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403729.7:c.-168C= MANE Select	ENSP00000385575.2:n.-168C=
ENST00000679571.1:c.-99C=	ENSP00000506307.1:n.-99C=
ENST00000681115.1:c.-168C=	ENSP00000505618.1:n.-168C=
ENST00000681710.1:c.-99C=	ENSP00000505865.1:n.-99C=
ENST00000403729.6:c.-168C=	ENSP00000385575.2:n.-168C=
ENST00000404191.5:c.-80+667C=	ENSP00000384028.1:n.-80+667C=
ENST00000506286.1:n.630-1074C=
ENST00000514959.1:n.248+6625C=
NM_001145794.1:c.-168C=	NP_001139266.1:n.-168C=
NM_001286780.1:c.-80+667C=	NP_001273709.1:n.-80+667C=
NM_001286781.1:c.-99C=	NP_001273710.1:n.-99C=
NM_058172.5:c.-168C=	NP_477520.2:n.-168C=
XM_011531587.1:c.-80+667C=	XP_011529889.1:n.-80+667C=
XM_011531587.3:c.-80+667C=	XP_011529889.1:n.-80+667C=
NM_058172.6:c.-168C= MANE Select	NP_477520.2:n.-168C=
NM_001286780.2:c.-80+667C=	NP_001273709.1:n.-80+667C=
NM_001286781.2:c.-99C=	NP_001273710.1:n.-99C=
NM_001145794.2:c.-168C=	NP_001139266.1:n.-168C=