Canonical Allele Identifier: CA1471242556
Gene: ANTXR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072649A= , CM000666.2:g.80072649A= GRCh38
NC_000004.11:g.80993803A= , CM000666.1:g.80993803A= GRCh37
NC_000004.10:g.81212827A= NCBI36
NG_015987.1:g.5675T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.-89T= MANE Select ENSP00000385575.2:n.-89T=
ENST00000679571.1:c.-80+60T= ENSP00000506307.1:n.-80+60T=
ENST00000680913.1:c.-89T= ENSP00000505640.1:n.-89T=
ENST00000681115.1:c.-89T= ENSP00000505618.1:n.-89T=
ENST00000681710.1:c.-80+60T= ENSP00000505865.1:n.-80+60T=
ENST00000346652.10:c.-89T= ENSP00000314883.6:n.-89T=
ENST00000403729.6:c.-89T= ENSP00000385575.2:n.-89T=
ENST00000404191.5:c.-80+746T= ENSP00000384028.1:n.-80+746T=
ENST00000506286.1:n.630-995T=
ENST00000514959.1:n.248+6704T=
NM_001145794.1:c.-89T= NP_001139266.1:n.-89T=
NM_001286780.1:c.-80+746T= NP_001273709.1:n.-80+746T=
NM_001286781.1:c.-80+60T= NP_001273710.1:n.-80+60T=
NM_058172.5:c.-89T= NP_477520.2:n.-89T=
XM_011531587.1:c.-80+746T= XP_011529889.1:n.-80+746T=
XM_011531587.3:c.-80+746T= XP_011529889.1:n.-80+746T=
NM_058172.6:c.-89T= MANE Select NP_477520.2:n.-89T=
NM_001286780.2:c.-80+746T= NP_001273709.1:n.-80+746T=
NM_001286781.2:c.-80+60T= NP_001273710.1:n.-80+60T=
NM_001145794.2:c.-89T= NP_001139266.1:n.-89T=