Canonical Allele Identifier: CA1881276628
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130489379A= , CM000671.2:g.130489379A= GRCh38
NC_000009.11:g.133364766A= , CM000671.1:g.133364766A= GRCh37
NC_000009.10:g.132354587A= NCBI36
NG_011542.1:g.49673A=

Transcript Alleles

HGVS Amino-acid change
ENST00000352480.10:c.885A= MANE Select ENSP00000253004.6:p.Leu295=
ENST00000352480.9:c.885A= ENSP00000253004.6:p.Leu295=
ENST00000372386.6:n.156A=
ENST00000372393.7:c.885A= ENSP00000361469.2:p.Leu295=
ENST00000372394.5:c.885A= ENSP00000361471.1:p.Leu295=
ENST00000470849.4:n.610A=
ENST00000492400.5:n.394A=
ENST00000493984.6:n.662A=
NM_000050.4:c.885A= NP_000041.2:p.Leu295=
NM_054012.3:c.885A= NP_446464.1:p.Leu295=
XM_005272200.2:c.885A= XP_005272257.1:p.Leu295=
XM_011518705.1:c.999A= XP_011517007.1:p.Leu333=
XM_005272200.3:c.885A= XP_005272257.1:p.Leu295=
XM_011518705.2:c.999A= XP_011517007.1:p.Leu333=
XM_017014729.1:c.981A= XP_016870218.1:p.Leu327=
NM_054012.4:c.885A= MANE Select NP_446464.1:p.Leu295=