Canonical Allele Identifier: CA1881255886
Gene: ASS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130470877G= , CM000671.2:g.130470877G= GRCh38
NC_000009.11:g.133346264G= , CM000671.1:g.133346264G= GRCh37
NC_000009.10:g.132336085G= NCBI36
NG_011542.1:g.31171G=

Transcript Alleles

HGVS Amino-acid Change
NM_054012.4:c.539G= MANE Select NP_446464.1:p.Ser180=
ENST00000352480.10:c.539G= MANE Select ENSP00000253004.6:p.Ser180=
NM_000050.4:c.539G= NP_000041.2:p.Ser180=
NM_054012.3:c.539G= NP_446464.1:p.Ser180=
ENST00000352480.9:c.539G= ENSP00000253004.6:p.Ser180=
ENST00000372393.7:c.539G= ENSP00000361469.2:p.Ser180=
ENST00000372394.5:c.539G= ENSP00000361471.1:p.Ser180=
ENST00000422569.5:c.539G= ENSP00000394212.1:p.Ser180=
ENST00000443588.1:c.482G= ENSP00000397785.1:p.Ser161=
ENST00000467695.5:n.248G=
ENST00000493984.6:n.370G=
XM_005272200.2:c.539G= XP_005272257.1:p.Ser180=
XM_005272200.3:c.539G= XP_005272257.1:p.Ser180=
XM_011518705.1:c.653G= XP_011517007.1:p.Ser218=
XM_011518705.2:c.653G= XP_011517007.1:p.Ser218=
XM_017014729.1:c.635G= XP_016870218.1:p.Ser212=