Canonical Allele Identifier: CA365649263
Gene: ARG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573333G>T , CM000668.2:g.131573333G>T GRCh38
NC_000006.11:g.131894473G>T , CM000668.1:g.131894473G>T GRCh37
NC_000006.10:g.131936166G>T NCBI36
NG_007086.2:g.5109G>T
NG_031860.1:g.59891C>A
NG_031860.2:g.59891C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368087.8:c.51G>T MANE Select ENSP00000357066.3:p.Lys17Asn
ENST00000640973.1:c.51G>T ENSP00000492623.1:p.Lys17Asn
ENST00000672052.1:n.305-3330G>T
ENST00000672233.1:c.77-5778G>T ENSP00000499826.1:n.77-5778G>T
ENST00000673234.1:c.77-3330G>T ENSP00000499885.1:n.77-3330G>T
ENST00000673427.1:c.51G>T ENSP00000500160.1:p.Lys17Asn
ENST00000275196.5:n.108G>T
ENST00000356962.2:c.51G>T ENSP00000349446.2:p.Lys17Asn
ENST00000368087.7:c.51G>T ENSP00000357066.3:p.Lys17Asn
ENST00000469293.1:n.140G>T
ENST00000498260.1:n.92G>T
NM_000045.3:c.51G>T NP_000036.2:p.Lys17Asn
NM_001244438.1:c.51G>T NP_001231367.1:p.Lys17Asn
XM_011535801.1:c.51G>T XP_011534103.1:p.Lys17Asn
XM_011535801.2:c.51G>T XP_011534103.1:p.Lys17Asn
NM_000045.4:c.51G>T MANE Select NP_000036.2:p.Lys17Asn
NM_001244438.2:c.51G>T NP_001231367.1:p.Lys17Asn
NM_001369020.1:c.51G>T NP_001355949.1:p.Lys17Asn
NR_160934.1:n.108G>T