Canonical Allele Identifier: CA1425997852

Gene: THPO EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184372875_184372878delinsTCAG , CM000665.2:g.184372875_184372878delinsTCAG	GRCh38
NC_000003.11:g.184090663_184090666delinsTCAG , CM000665.1:g.184090663_184090666delinsTCAG	GRCh37
NC_000003.10:g.185573357_185573360delinsTCAG	NCBI36
NG_012136.1:g.10267_10270delinsCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645603.2:c.1117_1120delinsCTGA (THPO)	ENSP00000494281.2:p.Leu373=
ENST00000647395.1:c.697_700delinsCTGA (THPO) MANE Select	ENSP00000494504.1:p.Leu233=
ENST00000649095.1:c.1117_1120delinsCTGA (THPO)	ENSP00000497904.1:p.Leu373=
ENST00000650229.1:c.680_683delinsCTGA (THPO)	ENSP00000497233.1:p.Ala227=
ENST00000204615.11:c.697_700delinsCTGA (THPO)	ENSP00000204615.7:p.Leu233=
ENST00000421442.2:c.581_584delinsCTGA (THPO)	ENSP00000411704.2:p.Ala194=
ENST00000444495.1:c.2106+228168_2106+228171delinsTCAG (EIF2B5)	ENSP00000409142.1:n.2106+228168_2106+228171delinsTCAG
ENST00000445696.6:c.685_688delinsCTGA (THPO)	ENSP00000410763.2:p.Leu229=
NM_000460.3:c.697_700delinsCTGA (THPO)	NP_000451.1:p.Leu233=
NM_001177597.2:c.685_688delinsCTGA (THPO)	NP_001171068.1:p.Leu229=
NM_001177598.2:c.680_683delinsCTGA (THPO)	NP_001171069.1:p.Ala227=
NM_001289997.1:c.581_584delinsCTGA (THPO)	NP_001276926.1:p.Ala194=
NM_001289998.1:c.697_700delinsCTGA (THPO)	NP_001276927.1:p.Leu233=
NM_001290003.1:c.1117_1120delinsCTGA (THPO)	NP_001276932.1:p.Leu373=
NM_001290022.1:c.685_688delinsCTGA (THPO)	NP_001276951.1:p.Leu229=
NM_001290026.1:c.680_683delinsCTGA (THPO)	NP_001276955.1:p.Ala227=
NM_001290027.1:c.581_584delinsCTGA (THPO)	NP_001276956.1:p.Ala194=
NM_001290028.1:c.697_700delinsCTGA (THPO)	NP_001276957.1:p.Leu233=
XM_011513113.1:c.989_992delinsCTGA (THPO)	XP_011511415.1:p.Ala330=
NM_000460.4:c.697_700delinsCTGA (THPO) MANE Select	NP_000451.1:p.Leu233=
XM_017007107.1:c.989_992delinsCTGA (THPO)	XP_016862596.1:p.Ala330=