Canonical Allele Identifier: CA377397931
Gene: ADK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74525311C>G , CM000672.2:g.74525311C>G GRCh38
NC_000010.10:g.76285069C>G , CM000672.1:g.76285069C>G GRCh37
NC_000010.9:g.75955075C>G NCBI36
NG_030484.1:g.379127C>G
NG_030484.2:g.379127C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286621.7:c.611C>G ENSP00000286621.3:p.Ser204Cys
ENST00000372734.5:c.560C>G ENSP00000361819.3:p.Ser187Cys
ENST00000539909.6:c.611C>G MANE Select ENSP00000443965.2:p.Ser204Cys
ENST00000541550.6:c.560C>G ENSP00000438321.2:p.Ser187Cys
ENST00000672394.1:c.335C>G ENSP00000500390.1:p.Ser112Cys
ENST00000672429.1:c.556-63971C>G ENSP00000500292.1:n.556-63971C>G
ENST00000672604.1:c.351C>G
ENST00000672920.1:c.*356C>G ENSP00000500141.1:n.*356C>G
ENST00000673027.1:c.506C>G ENSP00000500201.1:p.Ser169Cys
ENST00000673310.1:c.560C>G ENSP00000500097.1:p.Ser187Cys
ENST00000673352.1:c.611C>G ENSP00000500056.1:p.Ser204Cys
ENST00000286621.6:c.611C>G ENSP00000286621.2:p.Ser204Cys
ENST00000372734.3:c.560C>G ENSP00000361819.3:p.Ser187Cys
ENST00000539909.5:c.556-63971C>G ENSP00000443965.1:n.556-63971C>G
ENST00000541550.5:c.506C>G ENSP00000438321.1:p.Ser169Cys
NM_001123.3:c.560C>G NP_001114.2:p.Ser187Cys
NM_001202449.1:c.506C>G NP_001189378.1:p.Ser169Cys
NM_001202450.1:c.556-63971C>G NP_001189379.1:n.556-63971C>G
NM_006721.3:c.611C>G NP_006712.2:p.Ser204Cys
NR_120673.1:n.259+2455G>C
XM_011539297.1:c.527C>G XP_011537599.1:p.Ser176Cys
XM_017015698.1:c.611C>G XP_016871187.1:p.Ser204Cys
XM_017015699.1:c.416C>G XP_016871188.1:p.Ser139Cys
XM_017015700.1:c.611C>G XP_016871189.1:p.Ser204Cys
XM_017015701.1:c.505-63971C>G XP_016871190.1:n.505-63971C>G
XM_017015702.1:c.560C>G XP_016871191.1:p.Ser187Cys
XM_017015703.2:c.335C>G XP_016871192.1:p.Ser112Cys
XM_017015704.1:c.611C>G XP_016871193.1:p.Ser204Cys
XM_017015705.1:c.556-63971C>G XP_016871194.1:n.556-63971C>G
XM_017015706.1:c.560C>G XP_016871195.1:p.Ser187Cys
NM_001369123.1:c.611C>G NP_001356052.1:p.Ser204Cys
NM_001369124.1:c.505-63971C>G NP_001356053.1:n.505-63971C>G
NM_006721.4:c.611C>G MANE Select NP_006712.2:p.Ser204Cys
NM_001123.4:c.560C>G NP_001114.2:p.Ser187Cys
NM_001202449.2:c.506C>G NP_001189378.1:p.Ser169Cys
NM_001202450.2:c.556-63971C>G NP_001189379.1:n.556-63971C>G