Canonical Allele Identifier: CA2689206770

Gene: DOCK8

Linked Data

• gnomAD v4: 9-414708-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414709del , CM000671.2:g.414709del	GRCh38
NC_000009.11:g.414709del , CM000671.1:g.414709del	GRCh37
NC_000009.10:g.404709del	NCBI36
NG_017007.1:g.204845del , LRG_196:g.204845del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3231-73del	ENSP00000371766.2:n.3231-73del
ENST00000683406.1:n.52-73del
ENST00000685949.1:n.2319-73del
ENST00000432829.7:c.3531-73del MANE Select	ENSP00000394888.3:n.3531-73del
ENST00000382329.1:c.1932-73del	ENSP00000371766.1:n.1932-73del
ENST00000432829.6:c.3531-73del	ENSP00000394888.3:n.3531-73del
ENST00000453981.5:c.3327-73del	ENSP00000408464.2:n.3327-73del
ENST00000469391.5:c.3231-73del	ENSP00000419438.1:n.3231-73del
ENST00000495184.5:n.5486-73del
NM_001190458.1:c.3231-73del	NP_001177387.1:n.3231-73del
NM_001193536.1:c.3327-73del	NP_001180465.1:n.3327-73del
NM_203447.3:c.3531-73del , LRG_196t1:c.3531-73del	NP_982272.2:n.3531-73del
XM_011518045.1:c.3231-73del	XP_011516347.1:n.3231-73del
XM_011518046.1:c.3393-73del	XP_011516348.1:n.3393-73del
XM_011518047.1:c.3327-73del	XP_011516349.1:n.3327-73del
XM_011518048.1:c.3327-73del	XP_011516350.1:n.3327-73del
XM_011518049.1:c.1767-73del	XP_011516351.1:n.1767-73del
XM_011518045.3:c.3231-73del	XP_011516347.1:n.3231-73del
XM_011518046.2:c.3393-73del	XP_011516348.1:n.3393-73del
XM_011518047.3:c.3327-73del	XP_011516349.1:n.3327-73del
XM_011518048.2:c.3327-73del	XP_011516350.1:n.3327-73del
XM_011518049.2:c.1767-73del	XP_011516351.1:n.1767-73del
XM_017015173.1:c.3327-73del	XP_016870662.1:n.3327-73del
XM_017015174.1:c.3393-73del	XP_016870663.1:n.3393-73del
NM_001190458.2:c.3231-73del	NP_001177387.1:n.3231-73del
NM_001193536.2:c.3327-73del	NP_001180465.1:n.3327-73del
NM_203447.4:c.3531-73del MANE Select	NP_982272.2:n.3531-73del