Canonical Allele Identifier: CA2160932426
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741243G= , CM000676.2:g.104741243G= GRCh38
NC_000014.8:g.105207580G= , CM000676.1:g.105207580G= GRCh37
NC_000014.7:g.104278625G= NCBI36
NG_051175.1:g.22047G=

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.793G= ENSP00000518203.1:p.Gly265=
ENST00000330877.7:c.793G= MANE Select ENSP00000331260.2:p.Gly265=
ENST00000330877.6:c.793G= ENSP00000331260.2:p.Gly265=
ENST00000332972.9:c.922G= ENSP00000333019.5:p.Gly308=
ENST00000553540.5:c.905G= ENSP00000450759.1:n.905G=
ENST00000555486.5:c.858G= ENSP00000473778.1:n.858G=
ENST00000557582.5:n.1714G=
NM_152328.3:c.793G= NP_689541.1:p.Gly265=
NM_199165.1:c.922G= NP_954634.1:p.Gly308=
XM_006720026.2:c.796G= XP_006720089.1:p.Gly266=
XM_011536412.1:c.925G= XP_011534714.1:p.Gly309=
XM_011536413.1:c.610G= XP_011534715.1:p.Gly204=
XM_011536414.1:c.607G= XP_011534716.1:p.Gly203=
XM_011536415.1:c.178G= XP_011534717.1:p.Gly60=
NM_001320424.1:c.178G= NP_001307353.1:p.Gly60=
NM_152328.4:c.793G= NP_689541.1:p.Gly265=
NM_199165.2:c.922G= NP_954634.1:p.Gly308=
XM_006720026.3:c.796G= XP_006720089.1:p.Gly266=
XM_011536412.2:c.925G= XP_011534714.1:p.Gly309=
XR_001750917.1:n.466C=
NM_152328.5:c.793G= MANE Select NP_689541.1:p.Gly265=