Canonical Allele Identifier: CA1471220736
Gene: ANTXR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.80054342A= , CM000666.2:g.80054342A= GRCh38
NC_000004.11:g.80975496A= , CM000666.1:g.80975496A= GRCh37
NC_000004.10:g.81194520A= NCBI36
NG_015987.1:g.23982T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403729.7:c.566T= MANE Select ENSP00000385575.2:p.Ile189=
ENST00000679571.1:c.335T= ENSP00000506307.1:p.Ile112=
ENST00000680913.1:c.566T= ENSP00000505640.1:p.Ile189=
ENST00000681115.1:c.566T= ENSP00000505618.1:p.Ile189=
ENST00000681710.1:c.335T= ENSP00000505865.1:p.Ile112=
ENST00000307333.7:c.566T= ENSP00000306185.6:p.Ile189=
ENST00000346652.10:c.566T= ENSP00000314883.6:p.Ile189=
ENST00000403729.6:c.566T= ENSP00000385575.2:p.Ile189=
ENST00000404191.5:c.335T= ENSP00000384028.1:p.Ile112=
ENST00000449651.5:c.335T= ENSP00000413700.1:p.Ile112=
ENST00000514959.1:n.518T=
NM_001145794.1:c.566T= NP_001139266.1:p.Ile189=
NM_001286780.1:c.335T= NP_001273709.1:p.Ile112=
NM_001286781.1:c.335T= NP_001273710.1:p.Ile112=
NM_058172.5:c.566T= NP_477520.2:p.Ile189=
XM_011531587.1:c.335T= XP_011529889.1:p.Ile112=
XM_011531587.3:c.335T= XP_011529889.1:p.Ile112=
NM_058172.6:c.566T= MANE Select NP_477520.2:p.Ile189=
NM_001286780.2:c.335T= NP_001273709.1:p.Ile112=
NM_001286781.2:c.335T= NP_001273710.1:p.Ile112=
NM_001145794.2:c.566T= NP_001139266.1:p.Ile189=