Canonical Allele Identifier: CA2671171523
Gene: ANTXR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80072627dup , CM000666.2:g.80072627dup GRCh38
NC_000004.11:g.80993781dup , CM000666.1:g.80993781dup GRCh37
NC_000004.10:g.81212805dup NCBI36
NG_015987.1:g.5697dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000403729.7:c.-67dup MANE Select ENSP00000385575.2:n.-67dup
ENST00000679571.1:c.-80+82dup ENSP00000506307.1:n.-80+82dup
ENST00000680913.1:c.-67dup ENSP00000505640.1:n.-67dup
ENST00000681115.1:c.-67dup ENSP00000505618.1:n.-67dup
ENST00000681710.1:c.-80+82dup ENSP00000505865.1:n.-80+82dup
ENST00000346652.10:c.-67dup ENSP00000314883.6:n.-67dup
ENST00000403729.6:c.-67dup ENSP00000385575.2:n.-67dup
ENST00000404191.5:c.-80+768dup ENSP00000384028.1:n.-80+768dup
ENST00000506286.1:n.630-973dup
ENST00000514959.1:n.248+6726dup
NM_001145794.1:c.-67dup NP_001139266.1:n.-67dup
NM_001286780.1:c.-80+768dup NP_001273709.1:n.-80+768dup
NM_001286781.1:c.-80+82dup NP_001273710.1:n.-80+82dup
NM_058172.5:c.-67dup NP_477520.2:n.-67dup
XM_011531587.1:c.-80+768dup XP_011529889.1:n.-80+768dup
XM_011531587.3:c.-80+768dup XP_011529889.1:n.-80+768dup
NM_058172.6:c.-67dup MANE Select NP_477520.2:n.-67dup
NM_001286780.2:c.-80+768dup NP_001273709.1:n.-80+768dup
NM_001286781.2:c.-80+82dup NP_001273710.1:n.-80+82dup
NM_001145794.2:c.-67dup NP_001139266.1:n.-67dup