Canonical Allele Identifier: CA2680351449

Gene: ARG1

Linked Data

• gnomAD v4: 6-131573227-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573227T>G , CM000668.2:g.131573227T>G	GRCh38
NC_000006.11:g.131894367T>G , CM000668.1:g.131894367T>G	GRCh37
NC_000006.10:g.131936060T>G	NCBI36
NG_007086.2:g.5003T>G
NG_031860.1:g.59997A>C
NG_031860.2:g.59997A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368087.8:c.-56T>G MANE Select	ENSP00000357066.3:n.-56T>G
ENST00000672052.1:n.305-3436T>G
ENST00000672233.1:c.77-5884T>G	ENSP00000499826.1:n.77-5884T>G
ENST00000673234.1:c.77-3436T>G	ENSP00000499885.1:n.77-3436T>G
ENST00000275196.5:n.2T>G
ENST00000356962.2:c.-56T>G	ENSP00000349446.2:n.-56T>G
ENST00000368087.7:c.-56T>G	ENSP00000357066.3:n.-56T>G
ENST00000469293.1:n.34T>G
NM_000045.3:c.-56T>G	NP_000036.2:n.-56T>G
NM_001244438.1:c.-56T>G	NP_001231367.1:n.-56T>G
XM_011535801.1:c.-56T>G	XP_011534103.1:n.-56T>G
XM_011535801.2:c.-56T>G	XP_011534103.1:n.-56T>G
NM_000045.4:c.-56T>G MANE Select	NP_000036.2:n.-56T>G
NM_001244438.2:c.-56T>G	NP_001231367.1:n.-56T>G
NM_001369020.1:c.-56T>G	NP_001355949.1:n.-56T>G
NR_160934.1:n.2T>G