Canonical Allele Identifier: CA4957438

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.317028T>G , CM000671.2:g.317028T>G	GRCh38
NC_000009.11:g.317028T>G , CM000671.1:g.317028T>G	GRCh37
NC_000009.10:g.307028T>G	NCBI36
NG_017007.1:g.107164T>G , LRG_196:g.107164T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_203447.4:c.742-15T>G MANE Select	NP_982272.2:n.742-15T>G
ENST00000432829.7:c.742-15T>G MANE Select	ENSP00000394888.3:n.742-15T>G
NM_001190458.1:c.538-15T>G	NP_001177387.1:n.538-15T>G
NM_001190458.2:c.538-15T>G	NP_001177387.1:n.538-15T>G
NM_001193536.1:c.538-15T>G	NP_001180465.1:n.538-15T>G
NM_001193536.2:c.538-15T>G	NP_001180465.1:n.538-15T>G
NM_203447.3:c.742-15T>G , LRG_196t1:c.742-15T>G	NP_982272.2:n.742-15T>G
ENST00000382329.2:c.538-15T>G	ENSP00000371766.2:n.538-15T>G
ENST00000382341.5:n.637-15T>G
ENST00000432829.6:c.742-15T>G	ENSP00000394888.3:n.742-15T>G
ENST00000453981.5:c.538-15T>G	ENSP00000408464.2:n.538-15T>G
ENST00000454469.6:n.851-15T>G
ENST00000469391.5:c.538-15T>G	ENSP00000419438.1:n.538-15T>G
ENST00000474772.2:n.188-15T>G
ENST00000483757.5:c.538-15T>G	ENSP00000417691.1:n.538-15T>G
ENST00000483757.6:c.538-15T>G	ENSP00000417691.2:n.538-15T>G
ENST00000495184.5:n.603-15T>G
ENST00000524396.5:c.*705-15T>G	ENSP00000436628.1:n.*705-15T>G
XM_011518045.1:c.538-15T>G	XP_011516347.1:n.538-15T>G
XM_011518045.3:c.538-15T>G	XP_011516347.1:n.538-15T>G
XM_011518046.1:c.604-15T>G	XP_011516348.1:n.604-15T>G
XM_011518046.2:c.604-15T>G	XP_011516348.1:n.604-15T>G
XM_011518047.1:c.538-15T>G	XP_011516349.1:n.538-15T>G
XM_011518047.3:c.538-15T>G	XP_011516349.1:n.538-15T>G
XM_011518048.1:c.538-15T>G	XP_011516350.1:n.538-15T>G
XM_011518048.2:c.538-15T>G	XP_011516350.1:n.538-15T>G
XM_017015173.1:c.538-15T>G	XP_016870662.1:n.538-15T>G
XM_017015174.1:c.604-15T>G	XP_016870663.1:n.604-15T>G