Canonical Allele Identifier: CA2160932419
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741241T= , CM000676.2:g.104741241T= GRCh38
NC_000014.8:g.105207578T= , CM000676.1:g.105207578T= GRCh37
NC_000014.7:g.104278623T= NCBI36
NG_051175.1:g.22045T=

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.791T= ENSP00000518203.1:p.Phe264=
ENST00000330877.7:c.791T= MANE Select ENSP00000331260.2:p.Phe264=
ENST00000330877.6:c.791T= ENSP00000331260.2:p.Phe264=
ENST00000332972.9:c.920T= ENSP00000333019.5:p.Phe307=
ENST00000553540.5:c.903T= ENSP00000450759.1:n.903T=
ENST00000555486.5:c.856T= ENSP00000473778.1:n.856T=
ENST00000557582.5:n.1712T=
NM_152328.3:c.791T= NP_689541.1:p.Phe264=
NM_199165.1:c.920T= NP_954634.1:p.Phe307=
XM_006720026.2:c.794T= XP_006720089.1:p.Phe265=
XM_011536412.1:c.923T= XP_011534714.1:p.Phe308=
XM_011536413.1:c.608T= XP_011534715.1:p.Phe203=
XM_011536414.1:c.605T= XP_011534716.1:p.Phe202=
XM_011536415.1:c.176T= XP_011534717.1:p.Phe59=
NM_001320424.1:c.176T= NP_001307353.1:p.Phe59=
NM_152328.4:c.791T= NP_689541.1:p.Phe264=
NM_199165.2:c.920T= NP_954634.1:p.Phe307=
XM_006720026.3:c.794T= XP_006720089.1:p.Phe265=
XM_011536412.2:c.923T= XP_011534714.1:p.Phe308=
XR_001750917.1:n.468A=
NM_152328.5:c.791T= MANE Select NP_689541.1:p.Phe264=