Canonical Allele Identifier: CA2762343904
Gene: ANTXR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072651T>G , CM000666.2:g.80072651T>G GRCh38
NC_000004.11:g.80993805T>G , CM000666.1:g.80993805T>G GRCh37
NC_000004.10:g.81212829T>G NCBI36
NG_015987.1:g.5673A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.-91A>C MANE Select ENSP00000385575.2:n.-91A>C
ENST00000679571.1:c.-80+58A>C ENSP00000506307.1:n.-80+58A>C
ENST00000680913.1:c.-91A>C ENSP00000505640.1:n.-91A>C
ENST00000681115.1:c.-91A>C ENSP00000505618.1:n.-91A>C
ENST00000681710.1:c.-80+58A>C ENSP00000505865.1:n.-80+58A>C
ENST00000346652.10:c.-91A>C ENSP00000314883.6:n.-91A>C
ENST00000403729.6:c.-91A>C ENSP00000385575.2:n.-91A>C
ENST00000404191.5:c.-80+744A>C ENSP00000384028.1:n.-80+744A>C
ENST00000506286.1:n.630-997A>C
ENST00000514959.1:n.248+6702A>C
NM_001145794.1:c.-91A>C NP_001139266.1:n.-91A>C
NM_001286780.1:c.-80+744A>C NP_001273709.1:n.-80+744A>C
NM_001286781.1:c.-80+58A>C NP_001273710.1:n.-80+58A>C
NM_058172.5:c.-91A>C NP_477520.2:n.-91A>C
XM_011531587.1:c.-80+744A>C XP_011529889.1:n.-80+744A>C
XM_011531587.3:c.-80+744A>C XP_011529889.1:n.-80+744A>C
NM_058172.6:c.-91A>C MANE Select NP_477520.2:n.-91A>C
NM_001286780.2:c.-80+744A>C NP_001273709.1:n.-80+744A>C
NM_001286781.2:c.-80+58A>C NP_001273710.1:n.-80+58A>C
NM_001145794.2:c.-91A>C NP_001139266.1:n.-91A>C