Canonical Allele Identifier: CA356113311

Gene: DOK7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3473495G>C , CM000666.2:g.3473495G>C	GRCh38
NC_000004.11:g.3475222G>C , CM000666.1:g.3475222G>C	GRCh37
NC_000004.10:g.3445020G>C	NCBI36
NG_013072.2:g.15190G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_173660.5:c.190G>C MANE Select	NP_775931.3:p.Gly64Arg
ENST00000340083.6:c.190G>C MANE Select	ENSP00000344432.5:p.Gly64Arg
NM_001164673.1:c.190G>C	NP_001158145.1:p.Gly64Arg
NM_001164673.2:c.190G>C	NP_001158145.1:p.Gly64Arg
NM_001301071.1:c.190G>C	NP_001288000.1:p.Gly64Arg
NM_001301071.2:c.190G>C	NP_001288000.1:p.Gly64Arg
NM_001363811.1:c.100+9944G>C	NP_001350740.1:n.100+9944G>C
NM_001363811.2:c.100+9944G>C	NP_001350740.1:n.100+9944G>C
NM_173660.4:c.190G>C	NP_775931.3:p.Gly64Arg
ENST00000340083.5:c.190G>C	ENSP00000344432.5:p.Gly64Arg
ENST00000503688.5:n.165+9944G>C
ENST00000507039.5:c.190G>C	ENSP00000423614.1:p.Gly64Arg
ENST00000511267.5:n.209G>C
ENST00000643608.1:c.100+9944G>C	ENSP00000495701.1:n.100+9944G>C
XM_011513435.1:c.190G>C	XP_011511737.1:p.Gly64Arg
XM_011513435.2:c.190G>C	XP_011511737.1:p.Gly64Arg
XM_011513436.1:c.190G>C	XP_011511738.1:p.Gly64Arg
XM_011513437.1:c.-214G>C	XP_011511739.1:n.-214G>C
XM_011513437.2:c.-214G>C	XP_011511739.1:n.-214G>C