Canonical Allele Identifier: CA355461701

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184372800C>G , CM000665.2:g.184372800C>G GRCh38
NC_000003.11:g.184090588C>G , CM000665.1:g.184090588C>G GRCh37
NC_000003.10:g.185573282C>G NCBI36
NG_012136.1:g.10345G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645603.2:c.1195G>C (THPO) ENSP00000494281.2:p.Gly399Arg
ENST00000647395.1:c.775G>C (THPO) MANE Select ENSP00000494504.1:p.Gly259Arg
ENST00000649095.1:c.1195G>C (THPO) ENSP00000497904.1:p.Gly399Arg
ENST00000650229.1:c.758G>C (THPO) ENSP00000497233.1:p.Trp253Ser
ENST00000204615.11:c.775G>C (THPO) ENSP00000204615.7:p.Gly259Arg
ENST00000421442.2:c.659G>C (THPO) ENSP00000411704.2:p.Trp220Ser
ENST00000444495.1:c.2106+228093C>G (EIF2B5) ENSP00000409142.1:n.2106+228093C>G
ENST00000445696.6:c.763G>C (THPO) ENSP00000410763.2:p.Gly255Arg
NM_000460.3:c.775G>C (THPO) NP_000451.1:p.Gly259Arg
NM_001177597.2:c.763G>C (THPO) NP_001171068.1:p.Gly255Arg
NM_001177598.2:c.758G>C (THPO) NP_001171069.1:p.Trp253Ser
NM_001289997.1:c.659G>C (THPO) NP_001276926.1:p.Trp220Ser
NM_001289998.1:c.775G>C (THPO) NP_001276927.1:p.Gly259Arg
NM_001290003.1:c.1195G>C (THPO) NP_001276932.1:p.Gly399Arg
NM_001290022.1:c.763G>C (THPO) NP_001276951.1:p.Gly255Arg
NM_001290026.1:c.758G>C (THPO) NP_001276955.1:p.Trp253Ser
NM_001290027.1:c.659G>C (THPO) NP_001276956.1:p.Trp220Ser
NM_001290028.1:c.775G>C (THPO) NP_001276957.1:p.Gly259Arg
XM_011513113.1:c.1067G>C (THPO) XP_011511415.1:p.Trp356Ser
NM_000460.4:c.775G>C (THPO) MANE Select NP_000451.1:p.Gly259Arg
XM_017007107.1:c.1067G>C (THPO) XP_016862596.1:p.Trp356Ser