Canonical Allele Identifier: CA585864180

Gene: DOCK8

Linked Data

• dbSNP Id: rs1308650755
• gnomAD v2: 9-271573-GTGA-G
• gnomAD v3: 9-271573-GTGA-G
• gnomAD v4: 9-271573-GTGA-G
• MyVariant Identifiers: chr9:g.271574_271576del (hg19) ; chr9:g.271574_271576del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.271578_271580del , CM000671.2:g.271578_271580del	GRCh38
NC_000009.11:g.271578_271580del , CM000671.1:g.271578_271580del	GRCh37
NC_000009.10:g.261578_261580del	NCBI36
NG_017007.1:g.61714_61716del , LRG_196:g.61714_61716del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.-151-49_-151-47del	ENSP00000371766.2:n.-151-49_-151-47del
ENST00000682121.1:n.166-14883_166-14881del
ENST00000684166.1:n.163-49_163-47del
ENST00000684384.1:n.163-49_163-47del
ENST00000432829.7:c.54-49_54-47del MANE Select	ENSP00000394888.3:n.54-49_54-47del
ENST00000432829.6:c.54-49_54-47del	ENSP00000394888.3:n.54-49_54-47del
ENST00000454469.6:n.163-49_163-47del
ENST00000469197.5:c.54-49_54-47del	ENSP00000418587.1:n.54-49_54-47del
ENST00000479404.5:c.-151-49_-151-47del	ENSP00000417082.1:n.-151-49_-151-47del
ENST00000524396.5:c.*17-49_*17-47del	ENSP00000436628.1:n.*17-49_*17-47del
NM_203447.3:c.54-49_54-47del , LRG_196t1:c.54-49_54-47del	NP_982272.2:n.54-49_54-47del
XM_011518047.1:c.-151-49_-151-47del	XP_011516349.1:n.-151-49_-151-47del
XR_929404.1:n.88+1329_88+1331del
XR_929406.1:n.1333+2708_1333+2710del
XM_011518045.3:c.-151-49_-151-47del	XP_011516347.1:n.-151-49_-151-47del
XM_011518047.3:c.-151-49_-151-47del	XP_011516349.1:n.-151-49_-151-47del
XM_017015173.1:c.-151-49_-151-47del	XP_016870662.1:n.-151-49_-151-47del
NM_203447.4:c.54-49_54-47del MANE Select	NP_982272.2:n.54-49_54-47del