Canonical Allele Identifier: CA1434239870
Gene: DOK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3471412A= , CM000666.2:g.3471412A= GRCh38
NC_000004.11:g.3473139A= , CM000666.1:g.3473139A= GRCh37
NC_000004.10:g.3442937A= NCBI36
NG_013072.2:g.13107A=

Transcript Alleles

HGVS Amino-acid Change
NM_173660.5:c.101-1994A= MANE Select NP_775931.3:n.101-1994A=
ENST00000340083.6:c.101-1994A= MANE Select ENSP00000344432.5:n.101-1994A=
NM_001164673.1:c.101-1994A= NP_001158145.1:n.101-1994A=
NM_001164673.2:c.101-1994A= NP_001158145.1:n.101-1994A=
NM_001301071.1:c.101-1994A= NP_001288000.1:n.101-1994A=
NM_001301071.2:c.101-1994A= NP_001288000.1:n.101-1994A=
NM_001363811.1:c.100+7861A= NP_001350740.1:n.100+7861A=
NM_001363811.2:c.100+7861A= NP_001350740.1:n.100+7861A=
NM_173660.4:c.101-1994A= NP_775931.3:n.101-1994A=
ENST00000340083.5:c.101-1994A= ENSP00000344432.5:n.101-1994A=
ENST00000503688.5:n.165+7861A=
ENST00000507039.5:c.101-1994A= ENSP00000423614.1:n.101-1994A=
ENST00000511267.5:n.120-1994A=
ENST00000643608.1:c.100+7861A= ENSP00000495701.1:n.100+7861A=
XM_011513435.1:c.101-1994A= XP_011511737.1:n.101-1994A=
XM_011513435.2:c.101-1994A= XP_011511737.1:n.101-1994A=
XM_011513436.1:c.101-1994A= XP_011511738.1:n.101-1994A=
XM_011513437.1:c.-303-1994A= XP_011511739.1:n.-303-1994A=
XM_011513437.2:c.-303-1994A= XP_011511739.1:n.-303-1994A=