Canonical Allele Identifier: CA391240861
Gene: ADSS1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000710323.1:c.792C>G ENSP00000518203.1:p.Phe264Leu
ENST00000330877.7:c.792C>G MANE Select ENSP00000331260.2:p.Phe264Leu
ENST00000330877.6:c.792C>G ENSP00000331260.2:p.Phe264Leu
ENST00000332972.9:c.921C>G ENSP00000333019.5:p.Phe307Leu
ENST00000553540.5:c.904C>G ENSP00000450759.1:n.904C>G
ENST00000555486.5:c.857C>G ENSP00000473778.1:n.857C>G
ENST00000557582.5:n.1713C>G
NM_152328.3:c.792C>G NP_689541.1:p.Phe264Leu
NM_199165.1:c.921C>G NP_954634.1:p.Phe307Leu
XM_006720026.2:c.795C>G XP_006720089.1:p.Phe265Leu
XM_011536412.1:c.924C>G XP_011534714.1:p.Phe308Leu
XM_011536413.1:c.609C>G XP_011534715.1:p.Phe203Leu
XM_011536414.1:c.606C>G XP_011534716.1:p.Phe202Leu
XM_011536415.1:c.177C>G XP_011534717.1:p.Phe59Leu
NM_001320424.1:c.177C>G NP_001307353.1:p.Phe59Leu
NM_152328.4:c.792C>G NP_689541.1:p.Phe264Leu
NM_199165.2:c.921C>G NP_954634.1:p.Phe307Leu
XM_006720026.3:c.795C>G XP_006720089.1:p.Phe265Leu
XM_011536412.2:c.924C>G XP_011534714.1:p.Phe308Leu
XR_001750917.1:n.467G>C
NM_152328.5:c.792C>G MANE Select NP_689541.1:p.Phe264Leu