Canonical Allele Identifier: CA1471242773
Gene: ANTXR2 HGNC NCBI

Linked Data

dbSNP Id: rs1734876826

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072771_80072782del , CM000666.2:g.80072771_80072782del GRCh38
NC_000004.11:g.80993925_80993936del , CM000666.1:g.80993925_80993936del GRCh37
NC_000004.10:g.81212949_81212960del NCBI36
NG_015987.1:g.5548_5559del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.-216_-205del MANE Select ENSP00000385575.2:n.-216_-205del
ENST00000679571.1:c.-147_-136del ENSP00000506307.1:n.-147_-136del
ENST00000681115.1:c.-216_-205del ENSP00000505618.1:n.-216_-205del
ENST00000681710.1:c.-147_-136del ENSP00000505865.1:n.-147_-136del
ENST00000403729.6:c.-216_-205del ENSP00000385575.2:n.-216_-205del
ENST00000404191.5:c.-80+619_-80+630del ENSP00000384028.1:n.-80+619_-80+630del
ENST00000506286.1:n.630-1122_630-1111del
ENST00000514959.1:n.248+6577_248+6588del
NM_001145794.1:c.-216_-205del NP_001139266.1:n.-216_-205del
NM_001286780.1:c.-80+619_-80+630del NP_001273709.1:n.-80+619_-80+630del
NM_001286781.1:c.-147_-136del NP_001273710.1:n.-147_-136del
NM_058172.5:c.-216_-205del NP_477520.2:n.-216_-205del
XM_011531587.1:c.-80+619_-80+630del XP_011529889.1:n.-80+619_-80+630del
XM_011531587.3:c.-80+619_-80+630del XP_011529889.1:n.-80+619_-80+630del
NM_058172.6:c.-216_-205del MANE Select NP_477520.2:n.-216_-205del
NM_001286780.2:c.-80+619_-80+630del NP_001273709.1:n.-80+619_-80+630del
NM_001286781.2:c.-147_-136del NP_001273710.1:n.-147_-136del
NM_001145794.2:c.-216_-205del NP_001139266.1:n.-216_-205del