Canonical Allele Identifier: CA2829104

Gene: DOK7

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3485663G>A , CM000666.2:g.3485663G>A	GRCh38
NC_000004.11:g.3487390G>A , CM000666.1:g.3487390G>A	GRCh37
NC_000004.10:g.3457188G>A	NCBI36
NG_013072.2:g.27358G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_173660.5:c.652+5G>A MANE Select	NP_775931.3:n.652+5G>A
ENST00000340083.6:c.652+5G>A MANE Select	ENSP00000344432.5:n.652+5G>A
NM_001164673.1:c.641+5G>A	NP_001158145.1:n.641+5G>A
NM_001164673.2:c.641+5G>A	NP_001158145.1:n.641+5G>A
NM_001256896.1:c.-279+5G>A	NP_001243825.1:n.-279+5G>A
NM_001256896.2:c.-279+5G>A	NP_001243825.1:n.-279+5G>A
NM_001301071.1:c.652+5G>A	NP_001288000.1:n.652+5G>A
NM_001301071.2:c.652+5G>A	NP_001288000.1:n.652+5G>A
NM_001363811.1:c.220+5G>A	NP_001350740.1:n.220+5G>A
NM_001363811.2:c.220+5G>A	NP_001350740.1:n.220+5G>A
NM_173660.4:c.652+5G>A	NP_775931.3:n.652+5G>A
ENST00000340083.5:c.652+5G>A	ENSP00000344432.5:n.652+5G>A
ENST00000503688.5:n.285+5G>A
ENST00000507039.5:c.641+5G>A	ENSP00000423614.1:n.641+5G>A
ENST00000513995.1:n.310+5G>A
ENST00000515886.5:n.420+5G>A
ENST00000643608.1:c.220+5G>A	ENSP00000495701.1:n.220+5G>A
XM_011513435.1:c.652+5G>A	XP_011511737.1:n.652+5G>A
XM_011513435.2:c.652+5G>A	XP_011511737.1:n.652+5G>A
XM_011513436.1:c.652+5G>A	XP_011511738.1:n.652+5G>A
XM_011513437.1:c.238+5G>A	XP_011511739.1:n.238+5G>A
XM_011513437.2:c.238+5G>A	XP_011511739.1:n.238+5G>A