Canonical Allele Identifier: CA1826888781

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414634_414636delinsCTG , CM000671.2:g.414634_414636delinsCTG	GRCh38
NC_000009.11:g.414634_414636delinsCTG , CM000671.1:g.414634_414636delinsCTG	GRCh37
NC_000009.10:g.404634_404636delinsCTG	NCBI36
NG_017007.1:g.204770_204772delinsCTG , LRG_196:g.204770_204772delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3231-148_3231-146delinsCTG	ENSP00000371766.2:n.3231-148_3231-146delinsCTG
ENST00000683406.1:n.52-148_52-146delinsCTG
ENST00000685949.1:n.2319-148_2319-146delinsCTG
ENST00000432829.7:c.3531-148_3531-146delinsCTG MANE Select	ENSP00000394888.3:n.3531-148_3531-146delinsCTG
ENST00000382329.1:c.1932-148_1932-146delinsCTG	ENSP00000371766.1:n.1932-148_1932-146delinsCTG
ENST00000432829.6:c.3531-148_3531-146delinsCTG	ENSP00000394888.3:n.3531-148_3531-146delinsCTG
ENST00000453981.5:c.3327-148_3327-146delinsCTG	ENSP00000408464.2:n.3327-148_3327-146delinsCTG
ENST00000469391.5:c.3231-148_3231-146delinsCTG	ENSP00000419438.1:n.3231-148_3231-146delinsCTG
ENST00000495184.5:n.5486-148_5486-146delinsCTG
NM_001190458.1:c.3231-148_3231-146delinsCTG	NP_001177387.1:n.3231-148_3231-146delinsCTG
NM_001193536.1:c.3327-148_3327-146delinsCTG	NP_001180465.1:n.3327-148_3327-146delinsCTG
NM_203447.3:c.3531-148_3531-146delinsCTG , LRG_196t1:c.3531-148_3531-146delinsCTG	NP_982272.2:n.3531-148_3531-146delinsCTG
XM_011518045.1:c.3231-148_3231-146delinsCTG	XP_011516347.1:n.3231-148_3231-146delinsCTG
XM_011518046.1:c.3393-148_3393-146delinsCTG	XP_011516348.1:n.3393-148_3393-146delinsCTG
XM_011518047.1:c.3327-148_3327-146delinsCTG	XP_011516349.1:n.3327-148_3327-146delinsCTG
XM_011518048.1:c.3327-148_3327-146delinsCTG	XP_011516350.1:n.3327-148_3327-146delinsCTG
XM_011518049.1:c.1767-148_1767-146delinsCTG	XP_011516351.1:n.1767-148_1767-146delinsCTG
XM_011518045.3:c.3231-148_3231-146delinsCTG	XP_011516347.1:n.3231-148_3231-146delinsCTG
XM_011518046.2:c.3393-148_3393-146delinsCTG	XP_011516348.1:n.3393-148_3393-146delinsCTG
XM_011518047.3:c.3327-148_3327-146delinsCTG	XP_011516349.1:n.3327-148_3327-146delinsCTG
XM_011518048.2:c.3327-148_3327-146delinsCTG	XP_011516350.1:n.3327-148_3327-146delinsCTG
XM_011518049.2:c.1767-148_1767-146delinsCTG	XP_011516351.1:n.1767-148_1767-146delinsCTG
XM_017015173.1:c.3327-148_3327-146delinsCTG	XP_016870662.1:n.3327-148_3327-146delinsCTG
XM_017015174.1:c.3393-148_3393-146delinsCTG	XP_016870663.1:n.3393-148_3393-146delinsCTG
NM_001190458.2:c.3231-148_3231-146delinsCTG	NP_001177387.1:n.3231-148_3231-146delinsCTG
NM_001193536.2:c.3327-148_3327-146delinsCTG	NP_001180465.1:n.3327-148_3327-146delinsCTG
NM_203447.4:c.3531-148_3531-146delinsCTG MANE Select	NP_982272.2:n.3531-148_3531-146delinsCTG