Canonical Allele Identifier: CA2160932295
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741136G= , CM000676.2:g.104741136G= GRCh38
NC_000014.8:g.105207473G= , CM000676.1:g.105207473G= GRCh37
NC_000014.7:g.104278518G= NCBI36
NG_051175.1:g.21940G=

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.686G= ENSP00000518203.1:p.Arg229=
ENST00000330877.7:c.686G= MANE Select ENSP00000331260.2:p.Arg229=
ENST00000330877.6:c.686G= ENSP00000331260.2:p.Arg229=
ENST00000332972.9:c.815G= ENSP00000333019.5:p.Arg272=
ENST00000553540.5:c.798G= ENSP00000450759.1:n.798G=
ENST00000555486.5:c.751G= ENSP00000473778.1:n.751G=
ENST00000557582.5:n.1607G=
NM_152328.3:c.686G= NP_689541.1:p.Arg229=
NM_199165.1:c.815G= NP_954634.1:p.Arg272=
XM_006720026.2:c.689G= XP_006720089.1:p.Arg230=
XM_011536412.1:c.818G= XP_011534714.1:p.Arg273=
XM_011536413.1:c.503G= XP_011534715.1:p.Arg168=
XM_011536414.1:c.500G= XP_011534716.1:p.Arg167=
XM_011536415.1:c.71G= XP_011534717.1:p.Arg24=
NM_001320424.1:c.71G= NP_001307353.1:p.Arg24=
NM_152328.4:c.686G= NP_689541.1:p.Arg229=
NM_199165.2:c.815G= NP_954634.1:p.Arg272=
XM_006720026.3:c.689G= XP_006720089.1:p.Arg230=
XM_011536412.2:c.818G= XP_011534714.1:p.Arg273=
NM_152328.5:c.686G= MANE Select NP_689541.1:p.Arg229=