Canonical Allele Identifier: CA356114057

Gene: DOK7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3476340A>G , CM000666.2:g.3476340A>G	GRCh38
NC_000004.11:g.3478067A>G , CM000666.1:g.3478067A>G	GRCh37
NC_000004.10:g.3447865A>G	NCBI36
NG_013072.2:g.18035A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_173660.5:c.332-2A>G MANE Select	NP_775931.3:n.332-2A>G
ENST00000340083.6:c.332-2A>G MANE Select	ENSP00000344432.5:n.332-2A>G
NM_001164673.1:c.332-2A>G	NP_001158145.1:n.332-2A>G
NM_001164673.2:c.332-2A>G	NP_001158145.1:n.332-2A>G
NM_001301071.1:c.332-2A>G	NP_001288000.1:n.332-2A>G
NM_001301071.2:c.332-2A>G	NP_001288000.1:n.332-2A>G
NM_001363811.1:c.101-9199A>G	NP_001350740.1:n.101-9199A>G
NM_001363811.2:c.101-9199A>G	NP_001350740.1:n.101-9199A>G
NM_173660.4:c.332-2A>G	NP_775931.3:n.332-2A>G
ENST00000340083.5:c.332-2A>G	ENSP00000344432.5:n.332-2A>G
ENST00000503688.5:n.166-9199A>G
ENST00000507039.5:c.332-2A>G	ENSP00000423614.1:n.332-2A>G
ENST00000511267.5:n.351-2A>G
ENST00000643608.1:c.101-9199A>G	ENSP00000495701.1:n.101-9199A>G
XM_011513435.1:c.332-2A>G	XP_011511737.1:n.332-2A>G
XM_011513435.2:c.332-2A>G	XP_011511737.1:n.332-2A>G
XM_011513436.1:c.332-2A>G	XP_011511738.1:n.332-2A>G
XM_011513437.1:c.-72-2A>G	XP_011511739.1:n.-72-2A>G
XM_011513437.2:c.-72-2A>G	XP_011511739.1:n.-72-2A>G
XR_925062.1:n.51T>C