Canonical Allele Identifier: CA1425997794

Gene: THPO EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184372727G= , CM000665.2:g.184372727G=	GRCh38
NC_000003.11:g.184090515G= , CM000665.1:g.184090515G=	GRCh37
NC_000003.10:g.185573209G=	NCBI36
NG_012136.1:g.10418C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645603.2:c.1268C= (THPO)	ENSP00000494281.2:p.Ser423=
ENST00000647395.1:c.848C= (THPO) MANE Select	ENSP00000494504.1:p.Ser283=
ENST00000649095.1:c.1268C= (THPO)	ENSP00000497904.1:p.Ser423=
ENST00000650229.1:c.831C= (THPO)	ENSP00000497233.1:p.Leu277=
ENST00000204615.11:c.848C= (THPO)	ENSP00000204615.7:p.Ser283=
ENST00000421442.2:c.732C= (THPO)	ENSP00000411704.2:p.Leu244=
ENST00000444495.1:c.2106+228020G= (EIF2B5)	ENSP00000409142.1:n.2106+228020G=
ENST00000445696.6:c.836C= (THPO)	ENSP00000410763.2:p.Ser279=
NM_000460.3:c.848C= (THPO)	NP_000451.1:p.Ser283=
NM_001177597.2:c.836C= (THPO)	NP_001171068.1:p.Ser279=
NM_001177598.2:c.831C= (THPO)	NP_001171069.1:p.Leu277=
NM_001289997.1:c.732C= (THPO)	NP_001276926.1:p.Leu244=
NM_001289998.1:c.848C= (THPO)	NP_001276927.1:p.Ser283=
NM_001290003.1:c.1268C= (THPO)	NP_001276932.1:p.Ser423=
NM_001290022.1:c.836C= (THPO)	NP_001276951.1:p.Ser279=
NM_001290026.1:c.831C= (THPO)	NP_001276955.1:p.Leu277=
NM_001290027.1:c.732C= (THPO)	NP_001276956.1:p.Leu244=
NM_001290028.1:c.848C= (THPO)	NP_001276957.1:p.Ser283=
XM_011513113.1:c.1140C= (THPO)	XP_011511415.1:p.Leu380=
NM_000460.4:c.848C= (THPO) MANE Select	NP_000451.1:p.Ser283=
XM_017007107.1:c.1140C= (THPO)	XP_016862596.1:p.Leu380=