Canonical Allele Identifier: CA391240833
Gene: ADSS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104741237G>A , CM000676.2:g.104741237G>A GRCh38
NC_000014.8:g.105207574G>A , CM000676.1:g.105207574G>A GRCh37
NC_000014.7:g.104278619G>A NCBI36
NG_051175.1:g.22041G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.787G>A ENSP00000518203.1:p.Asp263Asn
ENST00000330877.7:c.787G>A MANE Select ENSP00000331260.2:p.Asp263Asn
ENST00000330877.6:c.787G>A ENSP00000331260.2:p.Asp263Asn
ENST00000332972.9:c.916G>A ENSP00000333019.5:p.Asp306Asn
ENST00000553540.5:c.899G>A ENSP00000450759.1:n.899G>A
ENST00000555486.5:c.852G>A ENSP00000473778.1:n.852G>A
ENST00000557582.5:n.1708G>A
NM_152328.3:c.787G>A NP_689541.1:p.Asp263Asn
NM_199165.1:c.916G>A NP_954634.1:p.Asp306Asn
XM_006720026.2:c.790G>A XP_006720089.1:p.Asp264Asn
XM_011536412.1:c.919G>A XP_011534714.1:p.Asp307Asn
XM_011536413.1:c.604G>A XP_011534715.1:p.Asp202Asn
XM_011536414.1:c.601G>A XP_011534716.1:p.Asp201Asn
XM_011536415.1:c.172G>A XP_011534717.1:p.Asp58Asn
NM_001320424.1:c.172G>A NP_001307353.1:p.Asp58Asn
NM_152328.4:c.787G>A NP_689541.1:p.Asp263Asn
NM_199165.2:c.916G>A NP_954634.1:p.Asp306Asn
XM_006720026.3:c.790G>A XP_006720089.1:p.Asp264Asn
XM_011536412.2:c.919G>A XP_011534714.1:p.Asp307Asn
XR_001750917.1:n.472C>T
NM_152328.5:c.787G>A MANE Select NP_689541.1:p.Asp263Asn