Canonical Allele Identifier: CA2828996

Gene: DOK7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3476447C>T , CM000666.2:g.3476447C>T	GRCh38
NC_000004.11:g.3478174C>T , CM000666.1:g.3478174C>T	GRCh37
NC_000004.10:g.3447972C>T	NCBI36
NG_013072.2:g.18142C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_173660.5:c.437C>T MANE Select	NP_775931.3:p.Pro146Leu
ENST00000340083.6:c.437C>T MANE Select	ENSP00000344432.5:p.Pro146Leu
NM_001164673.1:c.437C>T	NP_001158145.1:p.Pro146Leu
NM_001164673.2:c.437C>T	NP_001158145.1:p.Pro146Leu
NM_001301071.1:c.437C>T	NP_001288000.1:p.Pro146Leu
NM_001301071.2:c.437C>T	NP_001288000.1:p.Pro146Leu
NM_001363811.1:c.101-9092C>T	NP_001350740.1:n.101-9092C>T
NM_001363811.2:c.101-9092C>T	NP_001350740.1:n.101-9092C>T
NM_173660.4:c.437C>T	NP_775931.3:p.Pro146Leu
ENST00000340083.5:c.437C>T	ENSP00000344432.5:p.Pro146Leu
ENST00000503688.5:n.166-9092C>T
ENST00000507039.5:c.437C>T	ENSP00000423614.1:p.Pro146Leu
ENST00000511267.5:n.456C>T
ENST00000643608.1:c.101-9092C>T	ENSP00000495701.1:n.101-9092C>T
XM_011513435.1:c.437C>T	XP_011511737.1:p.Pro146Leu
XM_011513435.2:c.437C>T	XP_011511737.1:p.Pro146Leu
XM_011513436.1:c.437C>T	XP_011511738.1:p.Pro146Leu
XM_011513437.1:c.34C>T	XP_011511739.1:p.Arg12Trp
XM_011513437.2:c.34C>T	XP_011511739.1:p.Arg12Trp