Canonical Allele Identifier: CA437332081

Gene: THPO EIF2B5

Linked Data

• gnomAD v4: 3-184372987-T-C
• MyVariant Identifiers: chr3:g.184090775T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184372987T>C , CM000665.2:g.184372987T>C	GRCh38
NC_000003.11:g.184090775T>C , CM000665.1:g.184090775T>C	GRCh37
NC_000003.10:g.185573469T>C	NCBI36
NG_012136.1:g.10158A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645603.2:c.1008A>G (THPO)	ENSP00000494281.2:p.Pro336=
ENST00000647395.1:c.588A>G (THPO) MANE Select	ENSP00000494504.1:p.Pro196=
ENST00000649095.1:c.1008A>G (THPO)	ENSP00000497904.1:p.Pro336=
ENST00000650229.1:c.571A>G (THPO)	ENSP00000497233.1:p.Lys191Glu
ENST00000204615.11:c.588A>G (THPO)	ENSP00000204615.7:p.Pro196=
ENST00000421442.2:c.478-6A>G (THPO)	ENSP00000411704.2:n.478-6A>G
ENST00000444495.1:c.2106+228280T>C (EIF2B5)	ENSP00000409142.1:n.2106+228280T>C
ENST00000445696.6:c.576A>G (THPO)	ENSP00000410763.2:p.Pro192=
ENST00000477594.1:n.165-6A>G (THPO)
NM_000460.3:c.588A>G (THPO)	NP_000451.1:p.Pro196=
NM_001177597.2:c.576A>G (THPO)	NP_001171068.1:p.Pro192=
NM_001177598.2:c.571A>G (THPO)	NP_001171069.1:p.Lys191Glu
NM_001289997.1:c.478-6A>G (THPO)	NP_001276926.1:n.478-6A>G
NM_001289998.1:c.588A>G (THPO)	NP_001276927.1:p.Pro196=
NM_001290003.1:c.1008A>G (THPO)	NP_001276932.1:p.Pro336=
NM_001290022.1:c.576A>G (THPO)	NP_001276951.1:p.Pro192=
NM_001290026.1:c.571A>G (THPO)	NP_001276955.1:p.Lys191Glu
NM_001290027.1:c.478-6A>G (THPO)	NP_001276956.1:n.478-6A>G
NM_001290028.1:c.588A>G (THPO)	NP_001276957.1:p.Pro196=
XM_011513113.1:c.886-6A>G (THPO)	XP_011511415.1:n.886-6A>G
NM_000460.4:c.588A>G (THPO) MANE Select	NP_000451.1:p.Pro196=
XM_017007107.1:c.886-6A>G (THPO)	XP_016862596.1:n.886-6A>G