Canonical Allele Identifier: CA2160932418
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741233C= , CM000676.2:g.104741233C= GRCh38
NC_000014.8:g.105207570C= , CM000676.1:g.105207570C= GRCh37
NC_000014.7:g.104278615C= NCBI36
NG_051175.1:g.22037C=

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.783C= ENSP00000518203.1:p.Asp261=
ENST00000330877.7:c.783C= MANE Select ENSP00000331260.2:p.Asp261=
ENST00000330877.6:c.783C= ENSP00000331260.2:p.Asp261=
ENST00000332972.9:c.912C= ENSP00000333019.5:p.Asp304=
ENST00000553540.5:c.895C= ENSP00000450759.1:n.895C=
ENST00000555486.5:c.848C= ENSP00000473778.1:n.848C=
ENST00000557582.5:n.1704C=
NM_152328.3:c.783C= NP_689541.1:p.Asp261=
NM_199165.1:c.912C= NP_954634.1:p.Asp304=
XM_006720026.2:c.786C= XP_006720089.1:p.Asp262=
XM_011536412.1:c.915C= XP_011534714.1:p.Asp305=
XM_011536413.1:c.600C= XP_011534715.1:p.Asp200=
XM_011536414.1:c.597C= XP_011534716.1:p.Asp199=
XM_011536415.1:c.168C= XP_011534717.1:p.Asp56=
NM_001320424.1:c.168C= NP_001307353.1:p.Asp56=
NM_152328.4:c.783C= NP_689541.1:p.Asp261=
NM_199165.2:c.912C= NP_954634.1:p.Asp304=
XM_006720026.3:c.786C= XP_006720089.1:p.Asp262=
XM_011536412.2:c.915C= XP_011534714.1:p.Asp305=
XR_001750917.1:n.476G=
NM_152328.5:c.783C= MANE Select NP_689541.1:p.Asp261=