Canonical Allele Identifier: CA357472591
Gene: ANTXR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80054347T>G , CM000666.2:g.80054347T>G GRCh38
NC_000004.11:g.80975501T>G , CM000666.1:g.80975501T>G GRCh37
NC_000004.10:g.81194525T>G NCBI36
NG_015987.1:g.23977A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403729.7:c.561A>C MANE Select ENSP00000385575.2:p.Glu187Asp
ENST00000679571.1:c.330A>C ENSP00000506307.1:p.Glu110Asp
ENST00000680913.1:c.561A>C ENSP00000505640.1:p.Glu187Asp
ENST00000681115.1:c.561A>C ENSP00000505618.1:p.Glu187Asp
ENST00000681710.1:c.330A>C ENSP00000505865.1:p.Glu110Asp
ENST00000307333.7:c.561A>C ENSP00000306185.6:p.Glu187Asp
ENST00000346652.10:c.561A>C ENSP00000314883.6:p.Glu187Asp
ENST00000403729.6:c.561A>C ENSP00000385575.2:p.Glu187Asp
ENST00000404191.5:c.330A>C ENSP00000384028.1:p.Glu110Asp
ENST00000449651.5:c.330A>C ENSP00000413700.1:p.Glu110Asp
ENST00000514959.1:n.513A>C
NM_001145794.1:c.561A>C NP_001139266.1:p.Glu187Asp
NM_001286780.1:c.330A>C NP_001273709.1:p.Glu110Asp
NM_001286781.1:c.330A>C NP_001273710.1:p.Glu110Asp
NM_058172.5:c.561A>C NP_477520.2:p.Glu187Asp
XM_011531587.1:c.330A>C XP_011529889.1:p.Glu110Asp
XM_011531587.3:c.330A>C XP_011529889.1:p.Glu110Asp
NM_058172.6:c.561A>C MANE Select NP_477520.2:p.Glu187Asp
NM_001286780.2:c.330A>C NP_001273709.1:p.Glu110Asp
NM_001286781.2:c.330A>C NP_001273710.1:p.Glu110Asp
NM_001145794.2:c.561A>C NP_001139266.1:p.Glu187Asp