Canonical Allele Identifier: CA1664127835
Gene: ARG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573220C= , CM000668.2:g.131573220C= GRCh38
NC_000006.11:g.131894360C= , CM000668.1:g.131894360C= GRCh37
NC_000006.10:g.131936053C= NCBI36
NG_007086.2:g.4996C=
NG_031860.1:g.60004G=
NG_031860.2:g.60004G=

Transcript Alleles

HGVS Amino-acid change
ENST00000672052.1:n.305-3443C=
ENST00000672233.1:c.77-5891C= ENSP00000499826.1:n.77-5891C=
ENST00000673234.1:c.77-3443C= ENSP00000499885.1:n.77-3443C=
ENST00000368087.7:c.-63C= ENSP00000357066.3:n.-63C=
ENST00000469293.1:n.27C=
NM_000045.3:c.-63C= NP_000036.2:n.-63C=
NM_001244438.1:c.-63C= NP_001231367.1:n.-63C=
XM_011535801.1:c.-63C= XP_011534103.1:n.-63C=
XM_011535801.2:c.-63C= XP_011534103.1:n.-63C=