Canonical Allele Identifier: CA463677867

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.271633T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.271633T>A , CM000671.2:g.271633T>A	GRCh38
NC_000009.11:g.271633T>A , CM000671.1:g.271633T>A	GRCh37
NC_000009.10:g.261633T>A	NCBI36
NG_017007.1:g.61769T>A , LRG_196:g.61769T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.-145T>A	ENSP00000371766.2:n.-145T>A
ENST00000682121.1:n.166-14828T>A
ENST00000684166.1:n.169T>A
ENST00000684384.1:n.169T>A
ENST00000432829.7:c.60T>A MANE Select	ENSP00000394888.3:p.Ser20=
ENST00000432829.6:c.60T>A	ENSP00000394888.3:p.Ser20=
ENST00000454469.6:n.169T>A
ENST00000469197.5:c.60T>A	ENSP00000418587.1:p.Ser20=
ENST00000479404.5:c.-145T>A	ENSP00000417082.1:n.-145T>A
ENST00000524396.5:c.*23T>A	ENSP00000436628.1:n.*23T>A
NM_203447.3:c.60T>A , LRG_196t1:c.60T>A	NP_982272.2:p.Ser20=
XM_011518045.1:c.-145T>A	XP_011516347.1:n.-145T>A
XM_011518047.1:c.-145T>A	XP_011516349.1:n.-145T>A
XR_929404.1:n.88+1272A>T
XR_929406.1:n.1333+2651A>T
XM_011518045.3:c.-145T>A	XP_011516347.1:n.-145T>A
XM_011518047.3:c.-145T>A	XP_011516349.1:n.-145T>A
XM_017015173.1:c.-145T>A	XP_016870662.1:n.-145T>A
NM_203447.4:c.60T>A MANE Select	NP_982272.2:p.Ser20=