Canonical Allele Identifier: CA356115881

Gene: DOK7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3492757A>T , CM000666.2:g.3492757A>T	GRCh38
NC_000004.11:g.3494484A>T , CM000666.1:g.3494484A>T	GRCh37
NC_000004.10:g.3464282A>T	NCBI36
NG_013072.2:g.34452A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_173660.5:c.773-2A>T MANE Select	NP_775931.3:n.773-2A>T
ENST00000340083.6:c.773-2A>T MANE Select	ENSP00000344432.5:n.773-2A>T
NM_001164673.1:c.762-2A>T	NP_001158145.1:n.762-2A>T
NM_001164673.2:c.762-2A>T	NP_001158145.1:n.762-2A>T
NM_001256896.1:c.-158-2A>T	NP_001243825.1:n.-158-2A>T
NM_001256896.2:c.-158-2A>T	NP_001243825.1:n.-158-2A>T
NM_001301071.1:c.773-2A>T	NP_001288000.1:n.773-2A>T
NM_001301071.2:c.773-2A>T	NP_001288000.1:n.773-2A>T
NM_001363811.1:c.341-2A>T	NP_001350740.1:n.341-2A>T
NM_001363811.2:c.341-2A>T	NP_001350740.1:n.341-2A>T
NM_173660.4:c.773-2A>T	NP_775931.3:n.773-2A>T
ENST00000340083.5:c.773-2A>T	ENSP00000344432.5:n.773-2A>T
ENST00000503688.5:n.406-2A>T
ENST00000507039.5:c.762-2A>T	ENSP00000423614.1:n.762-2A>T
ENST00000513995.1:n.431-2A>T
ENST00000515886.5:n.541-2A>T
ENST00000643608.1:c.341-2A>T	ENSP00000495701.1:n.341-2A>T
XM_011513435.1:c.773-2A>T	XP_011511737.1:n.773-2A>T
XM_011513435.2:c.773-2A>T	XP_011511737.1:n.773-2A>T
XM_011513436.1:c.773-2A>T	XP_011511738.1:n.773-2A>T
XM_011513437.1:c.359-2A>T	XP_011511739.1:n.359-2A>T
XM_011513437.2:c.359-2A>T	XP_011511739.1:n.359-2A>T