Canonical Allele Identifier: CA372758954

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.304686C>A , CM000671.2:g.304686C>A	GRCh38
NC_000009.11:g.304686C>A , CM000671.1:g.304686C>A	GRCh37
NC_000009.10:g.294686C>A	NCBI36
NG_017007.1:g.94822C>A , LRG_196:g.94822C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_203447.4:c.510C>A MANE Select	NP_982272.2:p.Cys170Ter
ENST00000432829.7:c.510C>A MANE Select	ENSP00000394888.3:p.Cys170Ter
NM_001190458.1:c.306C>A	NP_001177387.1:p.Cys102Ter
NM_001190458.2:c.306C>A	NP_001177387.1:p.Cys102Ter
NM_001193536.1:c.306C>A	NP_001180465.1:p.Cys102Ter
NM_001193536.2:c.306C>A	NP_001180465.1:p.Cys102Ter
NM_203447.3:c.510C>A , LRG_196t1:c.510C>A	NP_982272.2:p.Cys170Ter
ENST00000382329.2:c.306C>A	ENSP00000371766.2:p.Cys102Ter
ENST00000382341.5:n.405C>A
ENST00000432829.6:c.510C>A	ENSP00000394888.3:p.Cys170Ter
ENST00000453981.5:c.306C>A	ENSP00000408464.2:p.Cys102Ter
ENST00000454469.6:n.619C>A
ENST00000469391.5:c.306C>A	ENSP00000419438.1:p.Cys102Ter
ENST00000478380.5:n.389C>A
ENST00000483757.5:c.306C>A	ENSP00000417691.1:p.Cys102Ter
ENST00000483757.6:c.306C>A	ENSP00000417691.2:p.Cys102Ter
ENST00000487230.5:c.306C>A	ENSP00000418318.1:p.Cys102Ter
ENST00000495184.5:n.371C>A
ENST00000524396.5:c.*473C>A	ENSP00000436628.1:n.*473C>A
ENST00000682249.1:c.306C>A	ENSP00000507731.1:p.Cys102Ter
ENST00000684384.1:n.619C>A
XM_011518045.1:c.306C>A	XP_011516347.1:p.Cys102Ter
XM_011518045.3:c.306C>A	XP_011516347.1:p.Cys102Ter
XM_011518046.1:c.372C>A	XP_011516348.1:p.Cys124Ter
XM_011518046.2:c.372C>A	XP_011516348.1:p.Cys124Ter
XM_011518047.1:c.306C>A	XP_011516349.1:p.Cys102Ter
XM_011518047.3:c.306C>A	XP_011516349.1:p.Cys102Ter
XM_011518048.1:c.306C>A	XP_011516350.1:p.Cys102Ter
XM_011518048.2:c.306C>A	XP_011516350.1:p.Cys102Ter
XM_017015173.1:c.306C>A	XP_016870662.1:p.Cys102Ter
XM_017015174.1:c.372C>A	XP_016870663.1:p.Cys124Ter