Canonical Allele Identifier: CA1664127832
Gene: ARG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131573219G= , CM000668.2:g.131573219G= GRCh38
NC_000006.11:g.131894359G= , CM000668.1:g.131894359G= GRCh37
NC_000006.10:g.131936052G= NCBI36
NG_007086.2:g.4995G=
NG_031860.1:g.60005C=
NG_031860.2:g.60005C=

Transcript Alleles

HGVS Amino-acid change
ENST00000672052.1:n.305-3444G=
ENST00000672233.1:c.77-5892G= ENSP00000499826.1:n.77-5892G=
ENST00000673234.1:c.77-3444G= ENSP00000499885.1:n.77-3444G=
ENST00000368087.7:c.-64G= ENSP00000357066.3:n.-64G=
ENST00000469293.1:n.26G=
NM_000045.3:c.-64G= NP_000036.2:n.-64G=
NM_001244438.1:c.-64G= NP_001231367.1:n.-64G=
XM_011535801.1:c.-64G= XP_011534103.1:n.-64G=
XM_011535801.2:c.-64G= XP_011534103.1:n.-64G=