Canonical Allele Identifier: CA278854
Community Standard Title: NM_173660.5(DOK7):c.55-1G>T
Gene: DOK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3463505G>T , CM000666.2:g.3463505G>T GRCh38
NC_000004.11:g.3465232G>T , CM000666.1:g.3465232G>T GRCh37
NC_000004.10:g.3435030G>T NCBI36
NG_013072.2:g.5200G>T

Transcript Alleles

HGVS Amino-acid Change
NM_173660.5:c.55-1G>T MANE Select NP_775931.3:n.55-1G>T
ENST00000340083.6:c.55-1G>T MANE Select ENSP00000344432.5:n.55-1G>T
NM_001164673.1:c.55-1G>T NP_001158145.1:n.55-1G>T
NM_001164673.2:c.55-1G>T NP_001158145.1:n.55-1G>T
NM_001301071.1:c.55-1G>T NP_001288000.1:n.55-1G>T
NM_001301071.2:c.55-1G>T NP_001288000.1:n.55-1G>T
NM_001363811.1:c.55-1G>T NP_001350740.1:n.55-1G>T
NM_001363811.2:c.55-1G>T NP_001350740.1:n.55-1G>T
NM_173660.4:c.55-1G>T NP_775931.3:n.55-1G>T
ENST00000340083.5:c.55-1G>T ENSP00000344432.5:n.55-1G>T
ENST00000503688.5:n.120-1G>T
ENST00000507039.5:c.55-1G>T ENSP00000423614.1:n.55-1G>T
ENST00000511267.5:n.119+76G>T
ENST00000643608.1:c.55-1G>T ENSP00000495701.1:n.55-1G>T
XM_011513435.1:c.55-1G>T XP_011511737.1:n.55-1G>T
XM_011513435.2:c.55-1G>T XP_011511737.1:n.55-1G>T
XM_011513436.1:c.55-1G>T XP_011511738.1:n.55-1G>T
XM_011513437.1:c.-349-1G>T XP_011511739.1:n.-349-1G>T
XM_011513437.2:c.-349-1G>T XP_011511739.1:n.-349-1G>T