Canonical Allele Identifier: CA356113804

Gene: DOK7

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3473637G>T , CM000666.2:g.3473637G>T	GRCh38
NC_000004.11:g.3475364G>T , CM000666.1:g.3475364G>T	GRCh37
NC_000004.10:g.3445162G>T	NCBI36
NG_013072.2:g.15332G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340083.6:c.331+1G>T MANE Select	ENSP00000344432.5:n.331+1G>T
ENST00000643608.1:c.100+10086G>T	ENSP00000495701.1:n.100+10086G>T
ENST00000340083.5:c.331+1G>T	ENSP00000344432.5:n.331+1G>T
ENST00000503688.5:n.165+10086G>T
ENST00000507039.5:c.331+1G>T	ENSP00000423614.1:n.331+1G>T
ENST00000511267.5:n.350+1G>T
NM_001164673.1:c.331+1G>T	NP_001158145.1:n.331+1G>T
NM_001301071.1:c.331+1G>T	NP_001288000.1:n.331+1G>T
NM_173660.4:c.331+1G>T	NP_775931.3:n.331+1G>T
XM_011513435.1:c.331+1G>T	XP_011511737.1:n.331+1G>T
XM_011513436.1:c.331+1G>T	XP_011511738.1:n.331+1G>T
XM_011513437.1:c.-73+1G>T	XP_011511739.1:n.-73+1G>T
NM_001363811.1:c.100+10086G>T	NP_001350740.1:n.100+10086G>T
XM_011513435.2:c.331+1G>T	XP_011511737.1:n.331+1G>T
XM_011513437.2:c.-73+1G>T	XP_011511739.1:n.-73+1G>T
NM_173660.5:c.331+1G>T MANE Select	NP_775931.3:n.331+1G>T
NM_001164673.2:c.331+1G>T	NP_001158145.1:n.331+1G>T
NM_001301071.2:c.331+1G>T	NP_001288000.1:n.331+1G>T
NM_001363811.2:c.100+10086G>T	NP_001350740.1:n.100+10086G>T