Canonical Allele Identifier: CA353467270
Gene: EOGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69004381G>T , CM000665.2:g.69004381G>T GRCh38
NC_000003.11:g.69053532G>T , CM000665.1:g.69053532G>T GRCh37
NC_000003.10:g.69136222G>T NCBI36
NG_042829.1:g.14514C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000383701.8:c.617C>A MANE Select ENSP00000373206.3:p.Ser206Ter
ENST00000295571.9:c.617C>A ENSP00000295571.5:p.Ser206Ter
ENST00000383701.7:c.617C>A ENSP00000373206.3:p.Ser206Ter
ENST00000403140.6:c.617C>A ENSP00000384124.2:p.Ser206Ter
ENST00000540764.5:c.617C>A ENSP00000443780.2:p.Ser206Ter
ENST00000540955.5:c.617C>A ENSP00000444264.2:p.Ser206Ter
NM_001278689.1:c.617C>A NP_001265618.1:p.Ser206Ter
NM_173654.2:c.617C>A NP_775925.1:p.Ser206Ter
NR_103826.1:n.1293C>A
XM_005264743.2:c.617C>A XP_005264800.1:p.Ser206Ter
XM_011533599.1:c.617C>A XP_011531901.1:p.Ser206Ter
XM_011533600.1:c.617C>A XP_011531902.1:p.Ser206Ter
XM_011533601.1:c.617C>A XP_011531903.1:p.Ser206Ter
XM_011533602.1:c.617C>A XP_011531904.1:p.Ser206Ter
XM_011533603.1:c.617C>A XP_011531905.1:p.Ser206Ter
XM_011533604.1:c.617C>A XP_011531906.1:p.Ser206Ter
XM_011533605.1:c.617C>A XP_011531907.1:p.Ser206Ter
XM_017006204.1:c.617C>A XP_016861693.1:p.Ser206Ter
XM_017006205.1:c.617C>A XP_016861694.1:p.Ser206Ter
XM_017006206.1:c.617C>A XP_016861695.1:p.Ser206Ter
XM_017006207.1:c.-12C>A XP_016861696.1:n.-12C>A
XM_017006208.1:c.617C>A XP_016861697.1:p.Ser206Ter
NM_001278689.2:c.617C>A MANE Select NP_001265618.1:p.Ser206Ter
NM_173654.3:c.617C>A NP_775925.1:p.Ser206Ter
NR_103826.2:n.1083C>A