Canonical Allele Identifier: CA2671171402
Gene: ANTXR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072338dup , CM000666.2:g.80072338dup GRCh38
NC_000004.11:g.80993492dup , CM000666.1:g.80993492dup GRCh37
NC_000004.10:g.81212516dup NCBI36
NG_015987.1:g.5986dup

Transcript Alleles

HGVS Amino-acid change
ENST00000403729.7:c.152+71dup MANE Select ENSP00000385575.2:n.152+71dup
ENST00000679571.1:c.-80+371dup ENSP00000506307.1:n.-80+371dup
ENST00000680913.1:c.152+71dup ENSP00000505640.1:n.152+71dup
ENST00000681115.1:c.152+71dup ENSP00000505618.1:n.152+71dup
ENST00000681710.1:c.-80+371dup ENSP00000505865.1:n.-80+371dup
ENST00000307333.7:c.152+71dup ENSP00000306185.6:n.152+71dup
ENST00000346652.10:c.152+71dup ENSP00000314883.6:n.152+71dup
ENST00000403729.6:c.152+71dup ENSP00000385575.2:n.152+71dup
ENST00000404191.5:c.-79-684dup ENSP00000384028.1:n.-79-684dup
ENST00000506286.1:n.630-684dup
ENST00000514959.1:n.248+7015dup
NM_001145794.1:c.152+71dup NP_001139266.1:n.152+71dup
NM_001286780.1:c.-79-684dup NP_001273709.1:n.-79-684dup
NM_001286781.1:c.-80+371dup NP_001273710.1:n.-80+371dup
NM_058172.5:c.152+71dup NP_477520.2:n.152+71dup
XM_011531587.1:c.-79-684dup XP_011529889.1:n.-79-684dup
XM_011531587.3:c.-79-684dup XP_011529889.1:n.-79-684dup
NM_058172.6:c.152+71dup MANE Select NP_477520.2:n.152+71dup
NM_001286780.2:c.-79-684dup NP_001273709.1:n.-79-684dup
NM_001286781.2:c.-80+371dup NP_001273710.1:n.-80+371dup
NM_001145794.2:c.152+71dup NP_001139266.1:n.152+71dup