Canonical Allele Identifier: CA375223562
Community Standard Title: NM_054012.4(ASS1):c.53C>G (p.Ser18Trp)
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130452281C>G , CM000671.2:g.130452281C>G GRCh38
NC_000009.11:g.133327668C>G , CM000671.1:g.133327668C>G GRCh37
NC_000009.10:g.132317489C>G NCBI36
NG_011542.1:g.12575C>G

Transcript Alleles

HGVS Amino-acid Change
NM_054012.4:c.53C>G MANE Select NP_446464.1:p.Ser18Trp
ENST00000352480.10:c.53C>G MANE Select ENSP00000253004.6:p.Ser18Trp
NM_000050.4:c.53C>G NP_000041.2:p.Ser18Trp
NM_054012.3:c.53C>G NP_446464.1:p.Ser18Trp
ENST00000352480.9:c.53C>G ENSP00000253004.6:p.Ser18Trp
ENST00000372393.7:c.53C>G ENSP00000361469.2:p.Ser18Trp
ENST00000372394.5:c.53C>G ENSP00000361471.1:p.Ser18Trp
ENST00000422569.5:c.53C>G ENSP00000394212.1:p.Ser18Trp
ENST00000443588.1:c.53C>G ENSP00000397785.1:p.Ser18Trp
XM_005272200.2:c.53C>G XP_005272257.1:p.Ser18Trp
XM_005272200.3:c.53C>G XP_005272257.1:p.Ser18Trp
XM_011518705.1:c.167C>G XP_011517007.1:p.Ser56Trp
XM_011518705.2:c.167C>G XP_011517007.1:p.Ser56Trp
XM_017014729.1:c.149C>G XP_016870218.1:p.Ser50Trp