Canonical Allele Identifier: CA2578126663
Gene: ANTXR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072748A>T , CM000666.2:g.80072748A>T GRCh38
NC_000004.11:g.80993902A>T , CM000666.1:g.80993902A>T GRCh37
NC_000004.10:g.81212926A>T NCBI36
NG_015987.1:g.5576T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.-188T>A MANE Select ENSP00000385575.2:n.-188T>A
ENST00000679571.1:c.-119T>A ENSP00000506307.1:n.-119T>A
ENST00000681115.1:c.-188T>A ENSP00000505618.1:n.-188T>A
ENST00000681710.1:c.-119T>A ENSP00000505865.1:n.-119T>A
ENST00000403729.6:c.-188T>A ENSP00000385575.2:n.-188T>A
ENST00000404191.5:c.-80+647T>A ENSP00000384028.1:n.-80+647T>A
ENST00000506286.1:n.630-1094T>A
ENST00000514959.1:n.248+6605T>A
NM_001145794.1:c.-188T>A NP_001139266.1:n.-188T>A
NM_001286780.1:c.-80+647T>A NP_001273709.1:n.-80+647T>A
NM_001286781.1:c.-119T>A NP_001273710.1:n.-119T>A
NM_058172.5:c.-188T>A NP_477520.2:n.-188T>A
XM_011531587.1:c.-80+647T>A XP_011529889.1:n.-80+647T>A
XM_011531587.3:c.-80+647T>A XP_011529889.1:n.-80+647T>A
NM_058172.6:c.-188T>A MANE Select NP_477520.2:n.-188T>A
NM_001286780.2:c.-80+647T>A NP_001273709.1:n.-80+647T>A
NM_001286781.2:c.-119T>A NP_001273710.1:n.-119T>A
NM_001145794.2:c.-188T>A NP_001139266.1:n.-188T>A