Canonical Allele Identifier: CA1425999336

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184376290C>T , CM000665.2:g.184376290C>T GRCh38
NC_000003.11:g.184094078C>T , CM000665.1:g.184094078C>T GRCh37
NC_000003.10:g.185576772C>T NCBI36
NG_012136.1:g.6855G>A
NG_029559.1:g.1218C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000645603.2:c.390G>A (THPO) ENSP00000494281.2:p.Arg130=
ENST00000647395.1:c.-31G>A (THPO) MANE Select ENSP00000494504.1:n.-31G>A
ENST00000649095.1:c.390G>A (THPO) ENSP00000497904.1:p.Arg130=
ENST00000204615.11:c.-31G>A (THPO) ENSP00000204615.7:n.-31G>A
ENST00000444495.1:c.2106+231583C>T (EIF2B5) ENSP00000409142.1:n.2106+231583C>T
ENST00000445696.6:c.-31G>A (THPO) ENSP00000410763.2:n.-31G>A
NM_000460.3:c.-31G>A (THPO) NP_000451.1:n.-31G>A
NM_001177597.2:c.-31G>A (THPO) NP_001171068.1:n.-31G>A
NM_001177598.2:c.-31G>A (THPO) NP_001171069.1:n.-31G>A
NM_001289997.1:c.-31G>A (THPO) NP_001276926.1:n.-31G>A
NM_001289998.1:c.-31G>A (THPO) NP_001276927.1:n.-31G>A
NM_001290003.1:c.390G>A (THPO) NP_001276932.1:p.Arg130=
NM_001290022.1:c.-31G>A (THPO) NP_001276951.1:n.-31G>A
NM_001290026.1:c.-31G>A (THPO) NP_001276955.1:n.-31G>A
NM_001290027.1:c.-31G>A (THPO) NP_001276956.1:n.-31G>A
NM_001290028.1:c.-31G>A (THPO) NP_001276957.1:n.-31G>A
XM_011513113.1:c.390G>A (THPO) XP_011511415.1:p.Arg130=
NM_000460.4:c.-31G>A (THPO) MANE Select NP_000451.1:n.-31G>A
XM_017007107.1:c.390G>A (THPO) XP_016862596.1:p.Arg130=