Canonical Allele Identifier: CA1664127855
Gene: ARG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573236G= , CM000668.2:g.131573236G= GRCh38
NC_000006.11:g.131894376G= , CM000668.1:g.131894376G= GRCh37
NC_000006.10:g.131936069G= NCBI36
NG_007086.2:g.5012G=
NG_031860.1:g.59988C=
NG_031860.2:g.59988C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368087.8:c.-47G= MANE Select ENSP00000357066.3:n.-47G=
ENST00000672052.1:n.305-3427G=
ENST00000672233.1:c.77-5875G= ENSP00000499826.1:n.77-5875G=
ENST00000673234.1:c.77-3427G= ENSP00000499885.1:n.77-3427G=
ENST00000673427.1:c.-47G= ENSP00000500160.1:n.-47G=
ENST00000275196.5:n.11G=
ENST00000356962.2:c.-47G= ENSP00000349446.2:n.-47G=
ENST00000368087.7:c.-47G= ENSP00000357066.3:n.-47G=
ENST00000469293.1:n.43G=
NM_000045.3:c.-47G= NP_000036.2:n.-47G=
NM_001244438.1:c.-47G= NP_001231367.1:n.-47G=
XM_011535801.1:c.-47G= XP_011534103.1:n.-47G=
XM_011535801.2:c.-47G= XP_011534103.1:n.-47G=
NM_000045.4:c.-47G= MANE Select NP_000036.2:n.-47G=
NM_001244438.2:c.-47G= NP_001231367.1:n.-47G=
NM_001369020.1:c.-47G= NP_001355949.1:n.-47G=
NR_160934.1:n.11G=