Canonical Allele Identifier: CA2689198171

Gene: DOCK8

Linked Data

• gnomAD v4: 9-271541-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.271541A>C , CM000671.2:g.271541A>C	GRCh38
NC_000009.11:g.271541A>C , CM000671.1:g.271541A>C	GRCh37
NC_000009.10:g.261541A>C	NCBI36
NG_017007.1:g.61677A>C , LRG_196:g.61677A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.-151-86A>C	ENSP00000371766.2:n.-151-86A>C
ENST00000682121.1:n.166-14920A>C
ENST00000684166.1:n.163-86A>C
ENST00000684384.1:n.163-86A>C
ENST00000432829.7:c.54-86A>C MANE Select	ENSP00000394888.3:n.54-86A>C
ENST00000432829.6:c.54-86A>C	ENSP00000394888.3:n.54-86A>C
ENST00000454469.6:n.163-86A>C
ENST00000469197.5:c.54-86A>C	ENSP00000418587.1:n.54-86A>C
ENST00000479404.5:c.-151-86A>C	ENSP00000417082.1:n.-151-86A>C
ENST00000524396.5:c.*17-86A>C	ENSP00000436628.1:n.*17-86A>C
NM_203447.3:c.54-86A>C , LRG_196t1:c.54-86A>C	NP_982272.2:n.54-86A>C
XM_011518047.1:c.-151-86A>C	XP_011516349.1:n.-151-86A>C
XR_929404.1:n.88+1364T>G
XR_929406.1:n.1333+2743T>G
XM_011518045.3:c.-151-86A>C	XP_011516347.1:n.-151-86A>C
XM_011518047.3:c.-151-86A>C	XP_011516349.1:n.-151-86A>C
XM_017015173.1:c.-151-86A>C	XP_016870662.1:n.-151-86A>C
NM_203447.4:c.54-86A>C MANE Select	NP_982272.2:n.54-86A>C