Canonical Allele Identifier: CA2160932298
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741143G= , CM000676.2:g.104741143G= GRCh38
NC_000014.8:g.105207480G= , CM000676.1:g.105207480G= GRCh37
NC_000014.7:g.104278525G= NCBI36
NG_051175.1:g.21947G=

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.693G= ENSP00000518203.1:p.Met231=
ENST00000330877.7:c.693G= MANE Select ENSP00000331260.2:p.Met231=
ENST00000330877.6:c.693G= ENSP00000331260.2:p.Met231=
ENST00000332972.9:c.822G= ENSP00000333019.5:p.Met274=
ENST00000553540.5:c.805G= ENSP00000450759.1:n.805G=
ENST00000555486.5:c.758G= ENSP00000473778.1:n.758G=
ENST00000557582.5:n.1614G=
NM_152328.3:c.693G= NP_689541.1:p.Met231=
NM_199165.1:c.822G= NP_954634.1:p.Met274=
XM_006720026.2:c.696G= XP_006720089.1:p.Met232=
XM_011536412.1:c.825G= XP_011534714.1:p.Met275=
XM_011536413.1:c.510G= XP_011534715.1:p.Met170=
XM_011536414.1:c.507G= XP_011534716.1:p.Met169=
XM_011536415.1:c.78G= XP_011534717.1:p.Met26=
NM_001320424.1:c.78G= NP_001307353.1:p.Met26=
NM_152328.4:c.693G= NP_689541.1:p.Met231=
NM_199165.2:c.822G= NP_954634.1:p.Met274=
XM_006720026.3:c.696G= XP_006720089.1:p.Met232=
XM_011536412.2:c.825G= XP_011534714.1:p.Met275=
NM_152328.5:c.693G= MANE Select NP_689541.1:p.Met231=