Canonical Allele Identifier: CA2160932423
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741242C= , CM000676.2:g.104741242C= GRCh38
NC_000014.8:g.105207579C= , CM000676.1:g.105207579C= GRCh37
NC_000014.7:g.104278624C= NCBI36
NG_051175.1:g.22046C=

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.792C= ENSP00000518203.1:p.Phe264=
ENST00000330877.7:c.792C= MANE Select ENSP00000331260.2:p.Phe264=
ENST00000330877.6:c.792C= ENSP00000331260.2:p.Phe264=
ENST00000332972.9:c.921C= ENSP00000333019.5:p.Phe307=
ENST00000553540.5:c.904C= ENSP00000450759.1:n.904C=
ENST00000555486.5:c.857C= ENSP00000473778.1:n.857C=
ENST00000557582.5:n.1713C=
NM_152328.3:c.792C= NP_689541.1:p.Phe264=
NM_199165.1:c.921C= NP_954634.1:p.Phe307=
XM_006720026.2:c.795C= XP_006720089.1:p.Phe265=
XM_011536412.1:c.924C= XP_011534714.1:p.Phe308=
XM_011536413.1:c.609C= XP_011534715.1:p.Phe203=
XM_011536414.1:c.606C= XP_011534716.1:p.Phe202=
XM_011536415.1:c.177C= XP_011534717.1:p.Phe59=
NM_001320424.1:c.177C= NP_001307353.1:p.Phe59=
NM_152328.4:c.792C= NP_689541.1:p.Phe264=
NM_199165.2:c.921C= NP_954634.1:p.Phe307=
XM_006720026.3:c.795C= XP_006720089.1:p.Phe265=
XM_011536412.2:c.924C= XP_011534714.1:p.Phe308=
XR_001750917.1:n.467G=
NM_152328.5:c.792C= MANE Select NP_689541.1:p.Phe264=