Canonical Allele Identifier: CA2567036881

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184375310_184375311insTCTT , CM000665.2:g.184375310_184375311insTCTT GRCh38
NC_000003.11:g.184093098_184093099insTCTT , CM000665.1:g.184093098_184093099insTCTT GRCh37
NC_000003.10:g.185575792_185575793insTCTT NCBI36
NG_012136.1:g.7834_7835insAAGA
NG_029559.1:g.238_239insTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645603.2:c.648+204_648+205insAAGA (THPO) ENSP00000494281.2:n.648+204_648+205insAAGA
ENST00000647395.1:c.228+204_228+205insAAGA (THPO) MANE Select ENSP00000494504.1:n.228+204_228+205insAAGA
ENST00000649095.1:c.648+204_648+205insAAGA (THPO) ENSP00000497904.1:n.648+204_648+205insAAGA
ENST00000650229.1:c.228+204_228+205insAAGA (THPO) ENSP00000497233.1:n.228+204_228+205insAAGA
ENST00000204615.11:c.228+204_228+205insAAGA (THPO) ENSP00000204615.7:n.228+204_228+205insAAGA
ENST00000421442.2:c.228+204_228+205insAAGA (THPO) ENSP00000411704.2:n.228+204_228+205insAAGA
ENST00000444495.1:c.2106+230603_2106+230604insTCTT (EIF2B5) ENSP00000409142.1:n.2106+230603_2106+230604insTCTT
ENST00000445696.6:c.228+204_228+205insAAGA (THPO) ENSP00000410763.2:n.228+204_228+205insAAGA
NM_000460.3:c.228+204_228+205insAAGA (THPO) NP_000451.1:n.228+204_228+205insAAGA
NM_001177597.2:c.228+204_228+205insAAGA (THPO) NP_001171068.1:n.228+204_228+205insAAGA
NM_001177598.2:c.228+204_228+205insAAGA (THPO) NP_001171069.1:n.228+204_228+205insAAGA
NM_001289997.1:c.228+204_228+205insAAGA (THPO) NP_001276926.1:n.228+204_228+205insAAGA
NM_001289998.1:c.228+204_228+205insAAGA (THPO) NP_001276927.1:n.228+204_228+205insAAGA
NM_001290003.1:c.648+204_648+205insAAGA (THPO) NP_001276932.1:n.648+204_648+205insAAGA
NM_001290022.1:c.228+204_228+205insAAGA (THPO) NP_001276951.1:n.228+204_228+205insAAGA
NM_001290026.1:c.228+204_228+205insAAGA (THPO) NP_001276955.1:n.228+204_228+205insAAGA
NM_001290027.1:c.228+204_228+205insAAGA (THPO) NP_001276956.1:n.228+204_228+205insAAGA
NM_001290028.1:c.228+204_228+205insAAGA (THPO) NP_001276957.1:n.228+204_228+205insAAGA
XM_011513113.1:c.648+204_648+205insAAGA (THPO) XP_011511415.1:n.648+204_648+205insAAGA
NM_000460.4:c.228+204_228+205insAAGA (THPO) MANE Select NP_000451.1:n.228+204_228+205insAAGA
XM_017007107.1:c.648+204_648+205insAAGA (THPO) XP_016862596.1:n.648+204_648+205insAAGA