Canonical Allele Identifier: CA355462474

Gene: THPO EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184090905T>G (hg19) ; chr3:g.184373117T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184373117T>G , CM000665.2:g.184373117T>G	GRCh38
NC_000003.11:g.184090905T>G , CM000665.1:g.184090905T>G	GRCh37
NC_000003.10:g.185573599T>G	NCBI36
NG_012136.1:g.10028A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645603.2:c.878A>C (THPO)	ENSP00000494281.2:p.Gln293Pro
ENST00000647395.1:c.458A>C (THPO) MANE Select	ENSP00000494504.1:p.Gln153Pro
ENST00000649095.1:c.878A>C (THPO)	ENSP00000497904.1:p.Gln293Pro
ENST00000650229.1:c.441A>C (THPO)	ENSP00000497233.1:p.Pro147=
ENST00000204615.11:c.458A>C (THPO)	ENSP00000204615.7:p.Gln153Pro
ENST00000421442.2:c.458A>C (THPO)	ENSP00000411704.2:p.Gln153Pro
ENST00000444495.1:c.2106+228410T>G (EIF2B5)	ENSP00000409142.1:n.2106+228410T>G
ENST00000445696.6:c.446A>C (THPO)	ENSP00000410763.2:p.Gln149Pro
ENST00000477594.1:n.145A>C (THPO)
NM_000460.3:c.458A>C (THPO)	NP_000451.1:p.Gln153Pro
NM_001177597.2:c.446A>C (THPO)	NP_001171068.1:p.Gln149Pro
NM_001177598.2:c.441A>C (THPO)	NP_001171069.1:p.Pro147=
NM_001289997.1:c.458A>C (THPO)	NP_001276926.1:p.Gln153Pro
NM_001289998.1:c.458A>C (THPO)	NP_001276927.1:p.Gln153Pro
NM_001290003.1:c.878A>C (THPO)	NP_001276932.1:p.Gln293Pro
NM_001290022.1:c.446A>C (THPO)	NP_001276951.1:p.Gln149Pro
NM_001290026.1:c.441A>C (THPO)	NP_001276955.1:p.Pro147=
NM_001290027.1:c.458A>C (THPO)	NP_001276956.1:p.Gln153Pro
NM_001290028.1:c.458A>C (THPO)	NP_001276957.1:p.Gln153Pro
XM_011513113.1:c.866A>C (THPO)	XP_011511415.1:p.Gln289Pro
NM_000460.4:c.458A>C (THPO) MANE Select	NP_000451.1:p.Gln153Pro
XM_017007107.1:c.866A>C (THPO)	XP_016862596.1:p.Gln289Pro