Canonical Allele Identifier: CA356117569

Gene: DOK7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3493201T>G , CM000666.2:g.3493201T>G	GRCh38
NC_000004.11:g.3494928T>G , CM000666.1:g.3494928T>G	GRCh37
NC_000004.10:g.3464726T>G	NCBI36
NG_013072.2:g.34896T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_173660.5:c.1215T>G MANE Select	NP_775931.3:p.Tyr405Ter
ENST00000340083.6:c.1215T>G MANE Select	ENSP00000344432.5:p.Tyr405Ter
NM_001164673.1:c.*436T>G	NP_001158145.1:n.*436T>G
NM_001164673.2:c.*436T>G	NP_001158145.1:n.*436T>G
NM_001256896.1:c.285T>G	NP_001243825.1:p.Tyr95Ter
NM_001256896.2:c.285T>G	NP_001243825.1:p.Tyr95Ter
NM_001301071.1:c.1215T>G	NP_001288000.1:p.Tyr405Ter
NM_001301071.2:c.1215T>G	NP_001288000.1:p.Tyr405Ter
NM_001363811.1:c.783T>G	NP_001350740.1:p.Tyr261Ter
NM_001363811.2:c.783T>G	NP_001350740.1:p.Tyr261Ter
NM_173660.4:c.1215T>G	NP_775931.3:p.Tyr405Ter
ENST00000340083.5:c.1215T>G	ENSP00000344432.5:p.Tyr405Ter
ENST00000507039.5:c.*436T>G	ENSP00000423614.1:n.*436T>G
ENST00000512714.1:n.407T>G
ENST00000515886.5:n.983T>G
ENST00000643608.1:c.783T>G	ENSP00000495701.1:p.Tyr261Ter
XM_011513435.1:c.1215T>G	XP_011511737.1:p.Tyr405Ter
XM_011513435.2:c.1215T>G	XP_011511737.1:p.Tyr405Ter
XM_011513436.1:c.1215T>G	XP_011511738.1:p.Tyr405Ter
XM_011513437.1:c.801T>G	XP_011511739.1:p.Tyr267Ter
XM_011513437.2:c.801T>G	XP_011511739.1:p.Tyr267Ter