Canonical Allele Identifier: CA2160932297
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741141A= , CM000676.2:g.104741141A= GRCh38
NC_000014.8:g.105207478A= , CM000676.1:g.105207478A= GRCh37
NC_000014.7:g.104278523A= NCBI36
NG_051175.1:g.21945A=

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.691A= ENSP00000518203.1:p.Met231=
ENST00000330877.7:c.691A= MANE Select ENSP00000331260.2:p.Met231=
ENST00000330877.6:c.691A= ENSP00000331260.2:p.Met231=
ENST00000332972.9:c.820A= ENSP00000333019.5:p.Met274=
ENST00000553540.5:c.803A= ENSP00000450759.1:n.803A=
ENST00000555486.5:c.756A= ENSP00000473778.1:n.756A=
ENST00000557582.5:n.1612A=
NM_152328.3:c.691A= NP_689541.1:p.Met231=
NM_199165.1:c.820A= NP_954634.1:p.Met274=
XM_006720026.2:c.694A= XP_006720089.1:p.Met232=
XM_011536412.1:c.823A= XP_011534714.1:p.Met275=
XM_011536413.1:c.508A= XP_011534715.1:p.Met170=
XM_011536414.1:c.505A= XP_011534716.1:p.Met169=
XM_011536415.1:c.76A= XP_011534717.1:p.Met26=
NM_001320424.1:c.76A= NP_001307353.1:p.Met26=
NM_152328.4:c.691A= NP_689541.1:p.Met231=
NM_199165.2:c.820A= NP_954634.1:p.Met274=
XM_006720026.3:c.694A= XP_006720089.1:p.Met232=
XM_011536412.2:c.823A= XP_011534714.1:p.Met275=
NM_152328.5:c.691A= MANE Select NP_689541.1:p.Met231=