Canonical Allele Identifier: CA2829063
Community Standard Title: NM_173660.5(DOK7):c.564G>A (p.Glu188=)
Gene: DOK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3485570G>A , CM000666.2:g.3485570G>A GRCh38
NC_000004.11:g.3487297G>A , CM000666.1:g.3487297G>A GRCh37
NC_000004.10:g.3457095G>A NCBI36
NG_013072.2:g.27265G>A

Transcript Alleles

HGVS Amino-acid Change
NM_173660.5:c.564G>A MANE Select NP_775931.3:p.Glu188=
ENST00000340083.6:c.564G>A MANE Select ENSP00000344432.5:p.Glu188=
NM_001164673.1:c.553G>A NP_001158145.1:p.Gly185Arg
NM_001164673.2:c.553G>A NP_001158145.1:p.Gly185Arg
NM_001256896.1:c.-367G>A NP_001243825.1:n.-367G>A
NM_001256896.2:c.-367G>A NP_001243825.1:n.-367G>A
NM_001301071.1:c.564G>A NP_001288000.1:p.Glu188=
NM_001301071.2:c.564G>A NP_001288000.1:p.Glu188=
NM_001363811.1:c.132G>A NP_001350740.1:p.Glu44=
NM_001363811.2:c.132G>A NP_001350740.1:p.Glu44=
NM_173660.4:c.564G>A NP_775931.3:p.Glu188=
ENST00000340083.5:c.564G>A ENSP00000344432.5:p.Glu188=
ENST00000503688.5:n.197G>A
ENST00000507039.5:c.553G>A ENSP00000423614.1:p.Gly185Arg
ENST00000513995.1:n.222G>A
ENST00000515886.5:n.332G>A
ENST00000643608.1:c.132G>A ENSP00000495701.1:p.Glu44=
XM_011513435.1:c.564G>A XP_011511737.1:p.Glu188=
XM_011513435.2:c.564G>A XP_011511737.1:p.Glu188=
XM_011513436.1:c.564G>A XP_011511738.1:p.Glu188=
XM_011513437.1:c.150G>A XP_011511739.1:p.Glu50=
XM_011513437.2:c.150G>A XP_011511739.1:p.Glu50=