Canonical Allele Identifier: CA1826910602

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.451995_452004delinsTTTTTTTTCC , CM000671.2:g.451995_452004delinsTTTTTTTTCC	GRCh38
NC_000009.11:g.451995_452004delinsTTTTTTTTCC , CM000671.1:g.451995_452004delinsTTTTTTTTCC	GRCh37
NC_000009.10:g.441995_442004delinsTTTTTTTTCC	NCBI36
NG_017007.1:g.242131_242140delinsTTTTTTTTCC , LRG_196:g.242131_242140delinsTTTTTTTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5662-16_5662-7delinsTTTTTTTTCC	ENSP00000371766.2:n.5662-16_5662-7delinsTTTTTTTTCC
ENST00000683406.1:n.2437-16_2437-7delinsTTTTTTTTCC
ENST00000684637.1:n.1643-16_1643-7delinsTTTTTTTTCC
ENST00000685949.1:n.4750-16_4750-7delinsTTTTTTTTCC
ENST00000432829.7:c.5962-16_5962-7delinsTTTTTTTTCC MANE Select	ENSP00000394888.3:n.5962-16_5962-7delinsTTTTTTTTCC
ENST00000382329.1:c.4363-16_4363-7delinsTTTTTTTTCC	ENSP00000371766.1:n.4363-16_4363-7delinsTTTTTTTTCC
ENST00000432829.6:c.5962-16_5962-7delinsTTTTTTTTCC	ENSP00000394888.3:n.5962-16_5962-7delinsTTTTTTTTCC
ENST00000453981.5:c.5758-16_5758-7delinsTTTTTTTTCC	ENSP00000408464.2:n.5758-16_5758-7delinsTTTTTTTTCC
ENST00000469391.5:c.5662-16_5662-7delinsTTTTTTTTCC	ENSP00000419438.1:n.5662-16_5662-7delinsTTTTTTTTCC
ENST00000495184.5:n.7917-16_7917-7delinsTTTTTTTTCC
NM_001190458.1:c.5662-16_5662-7delinsTTTTTTTTCC	NP_001177387.1:n.5662-16_5662-7delinsTTTTTTTTCC
NM_001193536.1:c.5758-16_5758-7delinsTTTTTTTTCC	NP_001180465.1:n.5758-16_5758-7delinsTTTTTTTTCC
NM_203447.3:c.5962-16_5962-7delinsTTTTTTTTCC , LRG_196t1:c.5962-16_5962-7delinsTTTTTTTTCC	NP_982272.2:n.5962-16_5962-7delinsTTTTTTTTCC
XM_011518045.1:c.5662-16_5662-7delinsTTTTTTTTCC	XP_011516347.1:n.5662-16_5662-7delinsTTTTTTTTCC
XM_011518046.1:c.5824-16_5824-7delinsTTTTTTTTCC	XP_011516348.1:n.5824-16_5824-7delinsTTTTTTTTCC
XM_011518047.1:c.5758-16_5758-7delinsTTTTTTTTCC	XP_011516349.1:n.5758-16_5758-7delinsTTTTTTTTCC
XM_011518048.1:c.5758-16_5758-7delinsTTTTTTTTCC	XP_011516350.1:n.5758-16_5758-7delinsTTTTTTTTCC
XM_011518049.1:c.4198-16_4198-7delinsTTTTTTTTCC	XP_011516351.1:n.4198-16_4198-7delinsTTTTTTTTCC
XM_011518045.3:c.5662-16_5662-7delinsTTTTTTTTCC	XP_011516347.1:n.5662-16_5662-7delinsTTTTTTTTCC
XM_011518046.2:c.5824-16_5824-7delinsTTTTTTTTCC	XP_011516348.1:n.5824-16_5824-7delinsTTTTTTTTCC
XM_011518047.3:c.5758-16_5758-7delinsTTTTTTTTCC	XP_011516349.1:n.5758-16_5758-7delinsTTTTTTTTCC
XM_011518048.2:c.5758-16_5758-7delinsTTTTTTTTCC	XP_011516350.1:n.5758-16_5758-7delinsTTTTTTTTCC
XM_011518049.2:c.4198-16_4198-7delinsTTTTTTTTCC	XP_011516351.1:n.4198-16_4198-7delinsTTTTTTTTCC
XM_017015173.1:c.5758-16_5758-7delinsTTTTTTTTCC	XP_016870662.1:n.5758-16_5758-7delinsTTTTTTTTCC
XM_017015174.1:c.5824-16_5824-7delinsTTTTTTTTCC	XP_016870663.1:n.5824-16_5824-7delinsTTTTTTTTCC
NM_001190458.2:c.5662-16_5662-7delinsTTTTTTTTCC	NP_001177387.1:n.5662-16_5662-7delinsTTTTTTTTCC
NM_001193536.2:c.5758-16_5758-7delinsTTTTTTTTCC	NP_001180465.1:n.5758-16_5758-7delinsTTTTTTTTCC
NM_203447.4:c.5962-16_5962-7delinsTTTTTTTTCC MANE Select	NP_982272.2:n.5962-16_5962-7delinsTTTTTTTTCC