Canonical Allele Identifier: CA2697553678

Gene: ARG1

Linked Data

• ClinVar Variation Id: 2695035
• ClinVar RCV Id: RCV003498073

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131573357dup , CM000668.2:g.131573357dup	GRCh38
NC_000006.11:g.131894497dup , CM000668.1:g.131894497dup	GRCh37
NC_000006.10:g.131936190dup	NCBI36
NG_007086.2:g.5133dup
NG_031860.1:g.59869dup
NG_031860.2:g.59869dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000368087.8:c.57+18dup MANE Select	ENSP00000357066.3:n.57+18dup
ENST00000640973.1:c.57+18dup	ENSP00000492623.1:n.57+18dup
ENST00000672052.1:n.305-3306dup
ENST00000672233.1:c.77-5754dup	ENSP00000499826.1:n.77-5754dup
ENST00000673234.1:c.77-3306dup	ENSP00000499885.1:n.77-3306dup
ENST00000673427.1:c.57+18dup	ENSP00000500160.1:n.57+18dup
ENST00000275196.5:n.114+18dup
ENST00000356962.2:c.57+18dup	ENSP00000349446.2:n.57+18dup
ENST00000368087.7:c.57+18dup	ENSP00000357066.3:n.57+18dup
ENST00000469293.1:n.146+18dup
ENST00000498260.1:n.98+18dup
NM_000045.3:c.57+18dup	NP_000036.2:n.57+18dup
NM_001244438.1:c.57+18dup	NP_001231367.1:n.57+18dup
XM_011535801.1:c.57+18dup	XP_011534103.1:n.57+18dup
XM_011535801.2:c.57+18dup	XP_011534103.1:n.57+18dup
NM_000045.4:c.57+18dup MANE Select	NP_000036.2:n.57+18dup
NM_001244438.2:c.57+18dup	NP_001231367.1:n.57+18dup
NM_001369020.1:c.57+18dup	NP_001355949.1:n.57+18dup
NR_160934.1:n.114+18dup