Canonical Allele Identifier: CA1664127907

Gene: ARG1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573275G= , CM000668.2:g.131573275G=	GRCh38
NC_000006.11:g.131894415G= , CM000668.1:g.131894415G=	GRCh37
NC_000006.10:g.131936108G=	NCBI36
NG_007086.2:g.5051G=
NG_031860.1:g.59949C=
NG_031860.2:g.59949C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.-8G= MANE Select	ENSP00000357066.3:n.-8G=
ENST00000672052.1:n.305-3388G=
ENST00000672233.1:c.77-5836G=	ENSP00000499826.1:n.77-5836G=
ENST00000673234.1:c.77-3388G=	ENSP00000499885.1:n.77-3388G=
ENST00000673427.1:c.-8G=	ENSP00000500160.1:n.-8G=
ENST00000275196.5:n.50G=
ENST00000356962.2:c.-8G=	ENSP00000349446.2:n.-8G=
ENST00000368087.7:c.-8G=	ENSP00000357066.3:n.-8G=
ENST00000469293.1:n.82G=
ENST00000498260.1:n.34G=
NM_000045.3:c.-8G=	NP_000036.2:n.-8G=
NM_001244438.1:c.-8G=	NP_001231367.1:n.-8G=
XM_011535801.1:c.-8G=	XP_011534103.1:n.-8G=
XM_011535801.2:c.-8G=	XP_011534103.1:n.-8G=
NM_000045.4:c.-8G= MANE Select	NP_000036.2:n.-8G=
NM_001244438.2:c.-8G=	NP_001231367.1:n.-8G=
NM_001369020.1:c.-8G=	NP_001355949.1:n.-8G=
NR_160934.1:n.50G=