Canonical Allele Identifier: CA2680351492

Gene: ARG1

Linked Data

• gnomAD v4: 6-131573442-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573442C>T , CM000668.2:g.131573442C>T	GRCh38
NC_000006.11:g.131894582C>T , CM000668.1:g.131894582C>T	GRCh37
NC_000006.10:g.131936275C>T	NCBI36
NG_007086.2:g.5218C>T
NG_031860.1:g.59782G>A
NG_031860.2:g.59782G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368087.8:c.57+103C>T MANE Select	ENSP00000357066.3:n.57+103C>T
ENST00000640973.1:c.57+103C>T	ENSP00000492623.1:n.57+103C>T
ENST00000672052.1:n.305-3221C>T
ENST00000672233.1:c.77-5669C>T	ENSP00000499826.1:n.77-5669C>T
ENST00000673234.1:c.77-3221C>T	ENSP00000499885.1:n.77-3221C>T
ENST00000673427.1:c.57+103C>T	ENSP00000500160.1:n.57+103C>T
ENST00000275196.5:n.114+103C>T
ENST00000356962.2:c.57+103C>T	ENSP00000349446.2:n.57+103C>T
ENST00000368087.7:c.57+103C>T	ENSP00000357066.3:n.57+103C>T
ENST00000469293.1:n.146+103C>T
ENST00000498260.1:n.98+103C>T
NM_000045.3:c.57+103C>T	NP_000036.2:n.57+103C>T
NM_001244438.1:c.57+103C>T	NP_001231367.1:n.57+103C>T
XM_011535801.1:c.57+103C>T	XP_011534103.1:n.57+103C>T
XM_011535801.2:c.57+103C>T	XP_011534103.1:n.57+103C>T
NM_000045.4:c.57+103C>T MANE Select	NP_000036.2:n.57+103C>T
NM_001244438.2:c.57+103C>T	NP_001231367.1:n.57+103C>T
NM_001369020.1:c.57+103C>T	NP_001355949.1:n.57+103C>T
NR_160934.1:n.114+103C>T