Canonical Allele Identifier: CA375225343
Community Standard Title: NM_054012.4(ASS1):c.350G>A (p.Gly117Asp)
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130458576G>A , CM000671.2:g.130458576G>A GRCh38
NC_000009.11:g.133333963G>A , CM000671.1:g.133333963G>A GRCh37
NC_000009.10:g.132323784G>A NCBI36
NG_011542.1:g.18870G>A

Transcript Alleles

HGVS Amino-acid Change
NM_054012.4:c.350G>A MANE Select NP_446464.1:p.Gly117Asp
ENST00000352480.10:c.350G>A MANE Select ENSP00000253004.6:p.Gly117Asp
NM_000050.4:c.350G>A NP_000041.2:p.Gly117Asp
NM_054012.3:c.350G>A NP_446464.1:p.Gly117Asp
ENST00000352480.9:c.350G>A ENSP00000253004.6:p.Gly117Asp
ENST00000372393.7:c.350G>A ENSP00000361469.2:p.Gly117Asp
ENST00000372394.5:c.350G>A ENSP00000361471.1:p.Gly117Asp
ENST00000422569.5:c.350G>A ENSP00000394212.1:p.Gly117Asp
ENST00000443588.1:c.350G>A ENSP00000397785.1:p.Gly117Asp
ENST00000467695.5:n.59G>A
XM_005272200.2:c.350G>A XP_005272257.1:p.Gly117Asp
XM_005272200.3:c.350G>A XP_005272257.1:p.Gly117Asp
XM_011518705.1:c.464G>A XP_011517007.1:p.Gly155Asp
XM_011518705.2:c.464G>A XP_011517007.1:p.Gly155Asp
XM_017014729.1:c.446G>A XP_016870218.1:p.Gly149Asp