Canonical Allele Identifier: CA1471242527
Gene: ANTXR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072637C= , CM000666.2:g.80072637C= GRCh38
NC_000004.11:g.80993791C= , CM000666.1:g.80993791C= GRCh37
NC_000004.10:g.81212815C= NCBI36
NG_015987.1:g.5687G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.-77G= MANE Select ENSP00000385575.2:n.-77G=
ENST00000679571.1:c.-80+72G= ENSP00000506307.1:n.-80+72G=
ENST00000680913.1:c.-77G= ENSP00000505640.1:n.-77G=
ENST00000681115.1:c.-77G= ENSP00000505618.1:n.-77G=
ENST00000681710.1:c.-80+72G= ENSP00000505865.1:n.-80+72G=
ENST00000346652.10:c.-77G= ENSP00000314883.6:n.-77G=
ENST00000403729.6:c.-77G= ENSP00000385575.2:n.-77G=
ENST00000404191.5:c.-80+758G= ENSP00000384028.1:n.-80+758G=
ENST00000506286.1:n.630-983G=
ENST00000514959.1:n.248+6716G=
NM_001145794.1:c.-77G= NP_001139266.1:n.-77G=
NM_001286780.1:c.-80+758G= NP_001273709.1:n.-80+758G=
NM_001286781.1:c.-80+72G= NP_001273710.1:n.-80+72G=
NM_058172.5:c.-77G= NP_477520.2:n.-77G=
XM_011531587.1:c.-80+758G= XP_011529889.1:n.-80+758G=
XM_011531587.3:c.-80+758G= XP_011529889.1:n.-80+758G=
NM_058172.6:c.-77G= MANE Select NP_477520.2:n.-77G=
NM_001286780.2:c.-80+758G= NP_001273709.1:n.-80+758G=
NM_001286781.2:c.-80+72G= NP_001273710.1:n.-80+72G=
NM_001145794.2:c.-77G= NP_001139266.1:n.-77G=