Canonical Allele Identifier: CA1881276615
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489341G= , CM000671.2:g.130489341G= GRCh38
NC_000009.11:g.133364728G= , CM000671.1:g.133364728G= GRCh37
NC_000009.10:g.132354549G= NCBI36
NG_011542.1:g.49635G=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.847G= MANE Select ENSP00000253004.6:p.Glu283=
ENST00000352480.9:c.847G= ENSP00000253004.6:p.Glu283=
ENST00000372386.6:n.118G=
ENST00000372393.7:c.847G= ENSP00000361469.2:p.Glu283=
ENST00000372394.5:c.847G= ENSP00000361471.1:p.Glu283=
ENST00000470849.4:n.572G=
ENST00000492400.5:n.356G=
ENST00000493984.6:n.624G=
NM_000050.4:c.847G= NP_000041.2:p.Glu283=
NM_054012.3:c.847G= NP_446464.1:p.Glu283=
XM_005272200.2:c.847G= XP_005272257.1:p.Glu283=
XM_011518705.1:c.961G= XP_011517007.1:p.Glu321=
XM_005272200.3:c.847G= XP_005272257.1:p.Glu283=
XM_011518705.2:c.961G= XP_011517007.1:p.Glu321=
XM_017014729.1:c.943G= XP_016870218.1:p.Glu315=
NM_054012.4:c.847G= MANE Select NP_446464.1:p.Glu283=