Canonical Allele Identifier: CA2671171622
Gene: ANTXR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072701_80072702del , CM000666.2:g.80072701_80072702del GRCh38
NC_000004.11:g.80993855_80993856del , CM000666.1:g.80993855_80993856del GRCh37
NC_000004.10:g.81212879_81212880del NCBI36
NG_015987.1:g.5623_5624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.-141_-140del MANE Select ENSP00000385575.2:n.-141_-140del
ENST00000679571.1:c.-80+8_-80+9del ENSP00000506307.1:n.-80+8_-80+9del
ENST00000680913.1:c.-141_-140del ENSP00000505640.1:n.-141_-140del
ENST00000681115.1:c.-141_-140del ENSP00000505618.1:n.-141_-140del
ENST00000681710.1:c.-80+8_-80+9del ENSP00000505865.1:n.-80+8_-80+9del
ENST00000403729.6:c.-141_-140del ENSP00000385575.2:n.-141_-140del
ENST00000404191.5:c.-80+694_-80+695del ENSP00000384028.1:n.-80+694_-80+695del
ENST00000506286.1:n.630-1047_630-1046del
ENST00000514959.1:n.248+6652_248+6653del
NM_001145794.1:c.-141_-140del NP_001139266.1:n.-141_-140del
NM_001286780.1:c.-80+694_-80+695del NP_001273709.1:n.-80+694_-80+695del
NM_001286781.1:c.-80+8_-80+9del NP_001273710.1:n.-80+8_-80+9del
NM_058172.5:c.-141_-140del NP_477520.2:n.-141_-140del
XM_011531587.1:c.-80+694_-80+695del XP_011529889.1:n.-80+694_-80+695del
XM_011531587.3:c.-80+694_-80+695del XP_011529889.1:n.-80+694_-80+695del
NM_058172.6:c.-141_-140del MANE Select NP_477520.2:n.-141_-140del
NM_001286780.2:c.-80+694_-80+695del NP_001273709.1:n.-80+694_-80+695del
NM_001286781.2:c.-80+8_-80+9del NP_001273710.1:n.-80+8_-80+9del
NM_001145794.2:c.-141_-140del NP_001139266.1:n.-141_-140del