Canonical Allele Identifier: CA1664128005

Gene: ARG1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573314T= , CM000668.2:g.131573314T=	GRCh38
NC_000006.11:g.131894454T= , CM000668.1:g.131894454T=	GRCh37
NC_000006.10:g.131936147T=	NCBI36
NG_007086.2:g.5090T=
NG_031860.1:g.59910A=
NG_031860.2:g.59910A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000045.4:c.32T= MANE Select	NP_000036.2:p.Ile11=
ENST00000368087.8:c.32T= MANE Select	ENSP00000357066.3:p.Ile11=
NM_000045.3:c.32T=	NP_000036.2:p.Ile11=
NM_001244438.1:c.32T=	NP_001231367.1:p.Ile11=
NM_001244438.2:c.32T=	NP_001231367.1:p.Ile11=
NM_001369020.1:c.32T=	NP_001355949.1:p.Ile11=
NR_160934.1:n.89T=
ENST00000275196.5:n.89T=
ENST00000356962.2:c.32T=	ENSP00000349446.2:p.Ile11=
ENST00000368087.7:c.32T=	ENSP00000357066.3:p.Ile11=
ENST00000469293.1:n.121T=
ENST00000498260.1:n.73T=
ENST00000640973.1:c.32T=	ENSP00000492623.1:p.Ile11=
ENST00000672052.1:n.305-3349T=
ENST00000672233.1:c.77-5797T=	ENSP00000499826.1:n.77-5797T=
ENST00000673234.1:c.77-3349T=	ENSP00000499885.1:n.77-3349T=
ENST00000673427.1:c.32T=	ENSP00000500160.1:p.Ile11=
XM_011535801.1:c.32T=	XP_011534103.1:p.Ile11=
XM_011535801.2:c.32T=	XP_011534103.1:p.Ile11=