Canonical Allele Identifier: CA1664127862
Gene: ARG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573240A= , CM000668.2:g.131573240A= GRCh38
NC_000006.11:g.131894380A= , CM000668.1:g.131894380A= GRCh37
NC_000006.10:g.131936073A= NCBI36
NG_007086.2:g.5016A=
NG_031860.1:g.59984T=
NG_031860.2:g.59984T=

Transcript Alleles

HGVS Amino-acid change
ENST00000368087.8:c.-43A= MANE Select ENSP00000357066.3:n.-43A=
ENST00000672052.1:n.305-3423A=
ENST00000672233.1:c.77-5871A= ENSP00000499826.1:n.77-5871A=
ENST00000673234.1:c.77-3423A= ENSP00000499885.1:n.77-3423A=
ENST00000673427.1:c.-43A= ENSP00000500160.1:n.-43A=
ENST00000275196.5:n.15A=
ENST00000356962.2:c.-43A= ENSP00000349446.2:n.-43A=
ENST00000368087.7:c.-43A= ENSP00000357066.3:n.-43A=
ENST00000469293.1:n.47A=
NM_000045.3:c.-43A= NP_000036.2:n.-43A=
NM_001244438.1:c.-43A= NP_001231367.1:n.-43A=
XM_011535801.1:c.-43A= XP_011534103.1:n.-43A=
XM_011535801.2:c.-43A= XP_011534103.1:n.-43A=
NM_000045.4:c.-43A= MANE Select NP_000036.2:n.-43A=
NM_001244438.2:c.-43A= NP_001231367.1:n.-43A=
NM_001369020.1:c.-43A= NP_001355949.1:n.-43A=
NR_160934.1:n.15A=