Canonical Allele Identifier: CA1664127863
Gene: ARG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573243G= , CM000668.2:g.131573243G= GRCh38
NC_000006.11:g.131894383G= , CM000668.1:g.131894383G= GRCh37
NC_000006.10:g.131936076G= NCBI36
NG_007086.2:g.5019G=
NG_031860.1:g.59981C=
NG_031860.2:g.59981C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368087.8:c.-40G= MANE Select ENSP00000357066.3:n.-40G=
ENST00000672052.1:n.305-3420G=
ENST00000672233.1:c.77-5868G= ENSP00000499826.1:n.77-5868G=
ENST00000673234.1:c.77-3420G= ENSP00000499885.1:n.77-3420G=
ENST00000673427.1:c.-40G= ENSP00000500160.1:n.-40G=
ENST00000275196.5:n.18G=
ENST00000356962.2:c.-40G= ENSP00000349446.2:n.-40G=
ENST00000368087.7:c.-40G= ENSP00000357066.3:n.-40G=
ENST00000469293.1:n.50G=
ENST00000498260.1:n.2G=
NM_000045.3:c.-40G= NP_000036.2:n.-40G=
NM_001244438.1:c.-40G= NP_001231367.1:n.-40G=
XM_011535801.1:c.-40G= XP_011534103.1:n.-40G=
XM_011535801.2:c.-40G= XP_011534103.1:n.-40G=
NM_000045.4:c.-40G= MANE Select NP_000036.2:n.-40G=
NM_001244438.2:c.-40G= NP_001231367.1:n.-40G=
NM_001369020.1:c.-40G= NP_001355949.1:n.-40G=
NR_160934.1:n.18G=