Canonical Allele Identifier: CA1425998175

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184373564C= , CM000665.2:g.184373564C= GRCh38
NC_000003.11:g.184091352C= , CM000665.1:g.184091352C= GRCh37
NC_000003.10:g.185574046C= NCBI36
NG_012136.1:g.9581G=

Transcript Alleles

HGVS Amino-acid Change
NM_000460.4:c.247G= (THPO) MANE Select NP_000451.1:p.Asp83=
ENST00000647395.1:c.247G= (THPO) MANE Select ENSP00000494504.1:p.Asp83=
NM_000460.3:c.247G= (THPO) NP_000451.1:p.Asp83=
NM_001177597.2:c.247G= (THPO) NP_001171068.1:p.Asp83=
NM_001177598.2:c.247G= (THPO) NP_001171069.1:p.Asp83=
NM_001289997.1:c.247G= (THPO) NP_001276926.1:p.Asp83=
NM_001289998.1:c.247G= (THPO) NP_001276927.1:p.Asp83=
NM_001290003.1:c.667G= (THPO) NP_001276932.1:p.Asp223=
NM_001290022.1:c.247G= (THPO) NP_001276951.1:p.Asp83=
NM_001290026.1:c.247G= (THPO) NP_001276955.1:p.Asp83=
NM_001290027.1:c.247G= (THPO) NP_001276956.1:p.Asp83=
NM_001290028.1:c.247G= (THPO) NP_001276957.1:p.Asp83=
ENST00000204615.11:c.247G= (THPO) ENSP00000204615.7:p.Asp83=
ENST00000421442.2:c.247G= (THPO) ENSP00000411704.2:p.Asp83=
ENST00000444495.1:c.2106+228857C= (EIF2B5) ENSP00000409142.1:n.2106+228857C=
ENST00000445696.6:c.247G= (THPO) ENSP00000410763.2:p.Asp83=
ENST00000645603.2:c.667G= (THPO) ENSP00000494281.2:p.Asp223=
ENST00000649095.1:c.667G= (THPO) ENSP00000497904.1:p.Asp223=
ENST00000650229.1:c.247G= (THPO) ENSP00000497233.1:p.Asp83=
XM_011513113.1:c.667G= (THPO) XP_011511415.1:p.Asp223=
XM_017007107.1:c.667G= (THPO) XP_016862596.1:p.Asp223=