Canonical Allele Identifier: CA1425998980

Gene: THPO EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184375471_184375475delinsAAGAC , CM000665.2:g.184375471_184375475delinsAAGAC	GRCh38
NC_000003.11:g.184093259_184093263delinsAAGAC , CM000665.1:g.184093259_184093263delinsAAGAC	GRCh37
NC_000003.10:g.185575953_185575957delinsAAGAC	NCBI36
NG_012136.1:g.7670_7674delinsGTCTT
NG_029559.1:g.399_403delinsAAGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645603.2:c.648+40_648+44delinsGTCTT (THPO)	ENSP00000494281.2:n.648+40_648+44delinsGTCTT
ENST00000647395.1:c.228+40_228+44delinsGTCTT (THPO) MANE Select	ENSP00000494504.1:n.228+40_228+44delinsGTCTT
ENST00000649095.1:c.648+40_648+44delinsGTCTT (THPO)	ENSP00000497904.1:n.648+40_648+44delinsGTCTT
ENST00000650229.1:c.228+40_228+44delinsGTCTT (THPO)	ENSP00000497233.1:n.228+40_228+44delinsGTCTT
ENST00000204615.11:c.228+40_228+44delinsGTCTT (THPO)	ENSP00000204615.7:n.228+40_228+44delinsGTCTT
ENST00000421442.2:c.228+40_228+44delinsGTCTT (THPO)	ENSP00000411704.2:n.228+40_228+44delinsGTCTT
ENST00000444495.1:c.2106+230764_2106+230768delinsAAGAC (EIF2B5)	ENSP00000409142.1:n.2106+230764_2106+230768delinsAAGAC
ENST00000445696.6:c.228+40_228+44delinsGTCTT (THPO)	ENSP00000410763.2:n.228+40_228+44delinsGTCTT
NM_000460.3:c.228+40_228+44delinsGTCTT (THPO)	NP_000451.1:n.228+40_228+44delinsGTCTT
NM_001177597.2:c.228+40_228+44delinsGTCTT (THPO)	NP_001171068.1:n.228+40_228+44delinsGTCTT
NM_001177598.2:c.228+40_228+44delinsGTCTT (THPO)	NP_001171069.1:n.228+40_228+44delinsGTCTT
NM_001289997.1:c.228+40_228+44delinsGTCTT (THPO)	NP_001276926.1:n.228+40_228+44delinsGTCTT
NM_001289998.1:c.228+40_228+44delinsGTCTT (THPO)	NP_001276927.1:n.228+40_228+44delinsGTCTT
NM_001290003.1:c.648+40_648+44delinsGTCTT (THPO)	NP_001276932.1:n.648+40_648+44delinsGTCTT
NM_001290022.1:c.228+40_228+44delinsGTCTT (THPO)	NP_001276951.1:n.228+40_228+44delinsGTCTT
NM_001290026.1:c.228+40_228+44delinsGTCTT (THPO)	NP_001276955.1:n.228+40_228+44delinsGTCTT
NM_001290027.1:c.228+40_228+44delinsGTCTT (THPO)	NP_001276956.1:n.228+40_228+44delinsGTCTT
NM_001290028.1:c.228+40_228+44delinsGTCTT (THPO)	NP_001276957.1:n.228+40_228+44delinsGTCTT
XM_011513113.1:c.648+40_648+44delinsGTCTT (THPO)	XP_011511415.1:n.648+40_648+44delinsGTCTT
NM_000460.4:c.228+40_228+44delinsGTCTT (THPO) MANE Select	NP_000451.1:n.228+40_228+44delinsGTCTT
XM_017007107.1:c.648+40_648+44delinsGTCTT (THPO)	XP_016862596.1:n.648+40_648+44delinsGTCTT