Canonical Allele Identifier: CA1471255209
Gene: ANTXR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.79984751A= , CM000666.2:g.79984751A= GRCh38
NC_000004.11:g.80905905A= , CM000666.1:g.80905905A= GRCh37
NC_000004.10:g.81124929A= NCBI36
NG_015987.1:g.93573T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403729.7:c.1086+68T= MANE Select ENSP00000385575.2:n.1086+68T=
ENST00000679571.1:c.855+68T= ENSP00000506307.1:n.855+68T=
ENST00000680913.1:c.1086+68T= ENSP00000505640.1:n.1086+68T=
ENST00000681115.1:c.1086+68T= ENSP00000505618.1:n.1086+68T=
ENST00000681710.1:c.855+68T= ENSP00000505865.1:n.855+68T=
ENST00000307333.7:c.1086+68T= ENSP00000306185.6:n.1086+68T=
ENST00000346652.10:c.777+68T= ENSP00000314883.6:n.777+68T=
ENST00000403729.6:c.1086+68T= ENSP00000385575.2:n.1086+68T=
ENST00000404191.5:c.855+68T= ENSP00000384028.1:n.855+68T=
ENST00000449651.5:c.*236+68T= ENSP00000413700.1:n.*236+68T=
NM_001145794.1:c.1086+68T= NP_001139266.1:n.1086+68T=
NM_001286780.1:c.855+68T= NP_001273709.1:n.855+68T=
NM_001286781.1:c.855+68T= NP_001273710.1:n.855+68T=
NM_058172.5:c.1086+68T= NP_477520.2:n.1086+68T=
XM_011531587.1:c.855+68T= XP_011529889.1:n.855+68T=
XM_011531587.3:c.855+68T= XP_011529889.1:n.855+68T=
NM_058172.6:c.1086+68T= MANE Select NP_477520.2:n.1086+68T=
NM_001286780.2:c.855+68T= NP_001273709.1:n.855+68T=
NM_001286781.2:c.855+68T= NP_001273710.1:n.855+68T=
NM_001145794.2:c.1086+68T= NP_001139266.1:n.1086+68T=