Canonical Allele Identifier: CA2160932299
Gene: ADSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741144G= , CM000676.2:g.104741144G= GRCh38
NC_000014.8:g.105207481G= , CM000676.1:g.105207481G= GRCh37
NC_000014.7:g.104278526G= NCBI36
NG_051175.1:g.21948G=

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.694G= ENSP00000518203.1:p.Val232=
ENST00000330877.7:c.694G= MANE Select ENSP00000331260.2:p.Val232=
ENST00000330877.6:c.694G= ENSP00000331260.2:p.Val232=
ENST00000332972.9:c.823G= ENSP00000333019.5:p.Val275=
ENST00000553540.5:c.806G= ENSP00000450759.1:n.806G=
ENST00000555486.5:c.759G= ENSP00000473778.1:n.759G=
ENST00000557582.5:n.1615G=
NM_152328.3:c.694G= NP_689541.1:p.Val232=
NM_199165.1:c.823G= NP_954634.1:p.Val275=
XM_006720026.2:c.697G= XP_006720089.1:p.Val233=
XM_011536412.1:c.826G= XP_011534714.1:p.Val276=
XM_011536413.1:c.511G= XP_011534715.1:p.Val171=
XM_011536414.1:c.508G= XP_011534716.1:p.Val170=
XM_011536415.1:c.79G= XP_011534717.1:p.Val27=
NM_001320424.1:c.79G= NP_001307353.1:p.Val27=
NM_152328.4:c.694G= NP_689541.1:p.Val232=
NM_199165.2:c.823G= NP_954634.1:p.Val275=
XM_006720026.3:c.697G= XP_006720089.1:p.Val233=
XM_011536412.2:c.826G= XP_011534714.1:p.Val276=
XR_001750917.1:n.565C=
NM_152328.5:c.694G= MANE Select NP_689541.1:p.Val232=