Canonical Allele Identifier: CA2671171586
Gene: ANTXR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072679_80072715del , CM000666.2:g.80072679_80072715del GRCh38
NC_000004.11:g.80993833_80993869del , CM000666.1:g.80993833_80993869del GRCh37
NC_000004.10:g.81212857_81212893del NCBI36
NG_015987.1:g.5616_5652del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.-148_-112del MANE Select ENSP00000385575.2:n.-148_-112del
ENST00000679571.1:c.-80+1_-80+37del
ENST00000681115.1:c.-148_-112del ENSP00000505618.1:n.-148_-112del
ENST00000681710.1:c.-80+1_-80+37del
ENST00000403729.6:c.-148_-112del ENSP00000385575.2:n.-148_-112del
ENST00000404191.5:c.-80+687_-80+723del ENSP00000384028.1:n.-80+687_-80+723del
ENST00000506286.1:n.630-1054_630-1018del
ENST00000514959.1:n.248+6645_248+6681del
NM_001145794.1:c.-148_-112del NP_001139266.1:n.-148_-112del
NM_001286780.1:c.-80+687_-80+723del NP_001273709.1:n.-80+687_-80+723del
NM_001286781.1:c.-80+1_-80+37del
NM_058172.5:c.-148_-112del NP_477520.2:n.-148_-112del
XM_011531587.1:c.-80+687_-80+723del XP_011529889.1:n.-80+687_-80+723del
XM_011531587.3:c.-80+687_-80+723del XP_011529889.1:n.-80+687_-80+723del
NM_058172.6:c.-148_-112del MANE Select NP_477520.2:n.-148_-112del
NM_001286780.2:c.-80+687_-80+723del NP_001273709.1:n.-80+687_-80+723del
NM_001286781.2:c.-80+1_-80+37del
NM_001145794.2:c.-148_-112del NP_001139266.1:n.-148_-112del