Canonical Allele Identifier: CA372769650

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.452022A>T (hg19) ; chr9:g.452022A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.452022A>T , CM000671.2:g.452022A>T	GRCh38
NC_000009.11:g.452022A>T , CM000671.1:g.452022A>T	GRCh37
NC_000009.10:g.442022A>T	NCBI36
NG_017007.1:g.242158A>T , LRG_196:g.242158A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5673A>T	ENSP00000371766.2:p.Glu1891Asp
ENST00000683406.1:n.2448A>T
ENST00000684637.1:n.1654A>T
ENST00000685949.1:n.4761A>T
ENST00000432829.7:c.5973A>T MANE Select	ENSP00000394888.3:p.Glu1991Asp
ENST00000382329.1:c.4374A>T	ENSP00000371766.1:p.Glu1458Asp
ENST00000432829.6:c.5973A>T	ENSP00000394888.3:p.Glu1991Asp
ENST00000453981.5:c.5769A>T	ENSP00000408464.2:p.Glu1923Asp
ENST00000469391.5:c.5673A>T	ENSP00000419438.1:p.Glu1891Asp
ENST00000495184.5:n.7928A>T
NM_001190458.1:c.5673A>T	NP_001177387.1:p.Glu1891Asp
NM_001193536.1:c.5769A>T	NP_001180465.1:p.Glu1923Asp
NM_203447.3:c.5973A>T , LRG_196t1:c.5973A>T	NP_982272.2:p.Glu1991Asp
XM_011518045.1:c.5673A>T	XP_011516347.1:p.Glu1891Asp
XM_011518046.1:c.5835A>T	XP_011516348.1:p.Glu1945Asp
XM_011518047.1:c.5769A>T	XP_011516349.1:p.Glu1923Asp
XM_011518048.1:c.5769A>T	XP_011516350.1:p.Glu1923Asp
XM_011518049.1:c.4209A>T	XP_011516351.1:p.Glu1403Asp
XM_011518045.3:c.5673A>T	XP_011516347.1:p.Glu1891Asp
XM_011518046.2:c.5835A>T	XP_011516348.1:p.Glu1945Asp
XM_011518047.3:c.5769A>T	XP_011516349.1:p.Glu1923Asp
XM_011518048.2:c.5769A>T	XP_011516350.1:p.Glu1923Asp
XM_011518049.2:c.4209A>T	XP_011516351.1:p.Glu1403Asp
XM_017015173.1:c.5769A>T	XP_016870662.1:p.Glu1923Asp
XM_017015174.1:c.5835A>T	XP_016870663.1:p.Glu1945Asp
NM_001190458.2:c.5673A>T	NP_001177387.1:p.Glu1891Asp
NM_001193536.2:c.5769A>T	NP_001180465.1:p.Glu1923Asp
NM_203447.4:c.5973A>T MANE Select	NP_982272.2:p.Glu1991Asp