Canonical Allele Identifier: CA1664128233

Gene: ARG1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573471G= , CM000668.2:g.131573471G=	GRCh38
NC_000006.11:g.131894611G= , CM000668.1:g.131894611G=	GRCh37
NC_000006.10:g.131936304G=	NCBI36
NG_007086.2:g.5247G=
NG_031860.1:g.59753C=
NG_031860.2:g.59753C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.57+132G= MANE Select	ENSP00000357066.3:n.57+132G=
ENST00000640973.1:c.57+132G=	ENSP00000492623.1:n.57+132G=
ENST00000672052.1:n.305-3192G=
ENST00000672233.1:c.77-5640G=	ENSP00000499826.1:n.77-5640G=
ENST00000673234.1:c.77-3192G=	ENSP00000499885.1:n.77-3192G=
ENST00000673427.1:c.57+132G=	ENSP00000500160.1:n.57+132G=
ENST00000275196.5:n.114+132G=
ENST00000356962.2:c.57+132G=	ENSP00000349446.2:n.57+132G=
ENST00000368087.7:c.57+132G=	ENSP00000357066.3:n.57+132G=
ENST00000469293.1:n.146+132G=
ENST00000498260.1:n.98+132G=
NM_000045.3:c.57+132G=	NP_000036.2:n.57+132G=
NM_001244438.1:c.57+132G=	NP_001231367.1:n.57+132G=
XM_011535801.1:c.57+132G=	XP_011534103.1:n.57+132G=
XM_011535801.2:c.57+132G=	XP_011534103.1:n.57+132G=
NM_000045.4:c.57+132G= MANE Select	NP_000036.2:n.57+132G=
NM_001244438.2:c.57+132G=	NP_001231367.1:n.57+132G=
NM_001369020.1:c.57+132G=	NP_001355949.1:n.57+132G=
NR_160934.1:n.114+132G=