Canonical Allele Identifier: CA391240866
Gene: ADSS1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.793G>C ENSP00000518203.1:p.Gly265Arg
ENST00000330877.7:c.793G>C MANE Select ENSP00000331260.2:p.Gly265Arg
ENST00000330877.6:c.793G>C ENSP00000331260.2:p.Gly265Arg
ENST00000332972.9:c.922G>C ENSP00000333019.5:p.Gly308Arg
ENST00000553540.5:c.905G>C ENSP00000450759.1:n.905G>C
ENST00000555486.5:c.858G>C ENSP00000473778.1:n.858G>C
ENST00000557582.5:n.1714G>C
NM_152328.3:c.793G>C NP_689541.1:p.Gly265Arg
NM_199165.1:c.922G>C NP_954634.1:p.Gly308Arg
XM_006720026.2:c.796G>C XP_006720089.1:p.Gly266Arg
XM_011536412.1:c.925G>C XP_011534714.1:p.Gly309Arg
XM_011536413.1:c.610G>C XP_011534715.1:p.Gly204Arg
XM_011536414.1:c.607G>C XP_011534716.1:p.Gly203Arg
XM_011536415.1:c.178G>C XP_011534717.1:p.Gly60Arg
NM_001320424.1:c.178G>C NP_001307353.1:p.Gly60Arg
NM_152328.4:c.793G>C NP_689541.1:p.Gly265Arg
NM_199165.2:c.922G>C NP_954634.1:p.Gly308Arg
XM_006720026.3:c.796G>C XP_006720089.1:p.Gly266Arg
XM_011536412.2:c.925G>C XP_011534714.1:p.Gly309Arg
XR_001750917.1:n.466C>G
NM_152328.5:c.793G>C MANE Select NP_689541.1:p.Gly265Arg