Canonical Allele Identifier: CA1425997845

Gene: THPO EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184372858G= , CM000665.2:g.184372858G=	GRCh38
NC_000003.11:g.184090646G= , CM000665.1:g.184090646G=	GRCh37
NC_000003.10:g.185573340G=	NCBI36
NG_012136.1:g.10287C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645603.2:c.1137C= (THPO)	ENSP00000494281.2:p.Ser379=
ENST00000647395.1:c.717C= (THPO) MANE Select	ENSP00000494504.1:p.Ser239=
ENST00000649095.1:c.1137C= (THPO)	ENSP00000497904.1:p.Ser379=
ENST00000650229.1:c.700C= (THPO)	ENSP00000497233.1:p.Pro234=
ENST00000204615.11:c.717C= (THPO)	ENSP00000204615.7:p.Ser239=
ENST00000421442.2:c.601C= (THPO)	ENSP00000411704.2:p.Pro201=
ENST00000444495.1:c.2106+228151G= (EIF2B5)	ENSP00000409142.1:n.2106+228151G=
ENST00000445696.6:c.705C= (THPO)	ENSP00000410763.2:p.Ser235=
NM_000460.3:c.717C= (THPO)	NP_000451.1:p.Ser239=
NM_001177597.2:c.705C= (THPO)	NP_001171068.1:p.Ser235=
NM_001177598.2:c.700C= (THPO)	NP_001171069.1:p.Pro234=
NM_001289997.1:c.601C= (THPO)	NP_001276926.1:p.Pro201=
NM_001289998.1:c.717C= (THPO)	NP_001276927.1:p.Ser239=
NM_001290003.1:c.1137C= (THPO)	NP_001276932.1:p.Ser379=
NM_001290022.1:c.705C= (THPO)	NP_001276951.1:p.Ser235=
NM_001290026.1:c.700C= (THPO)	NP_001276955.1:p.Pro234=
NM_001290027.1:c.601C= (THPO)	NP_001276956.1:p.Pro201=
NM_001290028.1:c.717C= (THPO)	NP_001276957.1:p.Ser239=
XM_011513113.1:c.1009C= (THPO)	XP_011511415.1:p.Pro337=
NM_000460.4:c.717C= (THPO) MANE Select	NP_000451.1:p.Ser239=
XM_017007107.1:c.1009C= (THPO)	XP_016862596.1:p.Pro337=