Canonical Allele Identifier: CA2734929

Linked Data

dbSNP Id: rs759793150

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184373072C>T , CM000665.2:g.184373072C>T GRCh38
NC_000003.11:g.184090860C>T , CM000665.1:g.184090860C>T GRCh37
NC_000003.10:g.185573554C>T NCBI36
NG_012136.1:g.10073G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645603.2:c.923G>A (THPO) ENSP00000494281.2:p.Gly308Glu
ENST00000647395.1:c.503G>A (THPO) MANE Select ENSP00000494504.1:p.Gly168Glu
ENST00000649095.1:c.923G>A (THPO) ENSP00000497904.1:p.Gly308Glu
ENST00000650229.1:c.486G>A (THPO) ENSP00000497233.1:p.Arg162=
ENST00000204615.11:c.503G>A (THPO) ENSP00000204615.7:p.Gly168Glu
ENST00000421442.2:c.477+26G>A (THPO) ENSP00000411704.2:n.477+26G>A
ENST00000444495.1:c.2106+228365C>T (EIF2B5) ENSP00000409142.1:n.2106+228365C>T
ENST00000445696.6:c.491G>A (THPO) ENSP00000410763.2:p.Gly164Glu
ENST00000477594.1:n.164+26G>A (THPO)
NM_000460.3:c.503G>A (THPO) NP_000451.1:p.Gly168Glu
NM_001177597.2:c.491G>A (THPO) NP_001171068.1:p.Gly164Glu
NM_001177598.2:c.486G>A (THPO) NP_001171069.1:p.Arg162=
NM_001289997.1:c.477+26G>A (THPO) NP_001276926.1:n.477+26G>A
NM_001289998.1:c.503G>A (THPO) NP_001276927.1:p.Gly168Glu
NM_001290003.1:c.923G>A (THPO) NP_001276932.1:p.Gly308Glu
NM_001290022.1:c.491G>A (THPO) NP_001276951.1:p.Gly164Glu
NM_001290026.1:c.486G>A (THPO) NP_001276955.1:p.Arg162=
NM_001290027.1:c.477+26G>A (THPO) NP_001276956.1:n.477+26G>A
NM_001290028.1:c.503G>A (THPO) NP_001276957.1:p.Gly168Glu
XM_011513113.1:c.885+26G>A (THPO) XP_011511415.1:n.885+26G>A
NM_000460.4:c.503G>A (THPO) MANE Select NP_000451.1:p.Gly168Glu
XM_017007107.1:c.885+26G>A (THPO) XP_016862596.1:n.885+26G>A