Canonical Allele Identifier: CA372760625

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.414864C>A (hg19) ; chr9:g.414864C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414864C>A , CM000671.2:g.414864C>A	GRCh38
NC_000009.11:g.414864C>A , CM000671.1:g.414864C>A	GRCh37
NC_000009.10:g.404864C>A	NCBI36
NG_017007.1:g.205000C>A , LRG_196:g.205000C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3313C>A	ENSP00000371766.2:p.Pro1105Thr
ENST00000683406.1:n.134C>A
ENST00000685949.1:n.2401C>A
ENST00000432829.7:c.3613C>A MANE Select	ENSP00000394888.3:p.Pro1205Thr
ENST00000382329.1:c.2014C>A	ENSP00000371766.1:p.Pro672Thr
ENST00000432829.6:c.3613C>A	ENSP00000394888.3:p.Pro1205Thr
ENST00000453981.5:c.3409C>A	ENSP00000408464.2:p.Pro1137Thr
ENST00000469391.5:c.3313C>A	ENSP00000419438.1:p.Pro1105Thr
ENST00000495184.5:n.5568C>A
NM_001190458.1:c.3313C>A	NP_001177387.1:p.Pro1105Thr
NM_001193536.1:c.3409C>A	NP_001180465.1:p.Pro1137Thr
NM_203447.3:c.3613C>A , LRG_196t1:c.3613C>A	NP_982272.2:p.Pro1205Thr
XM_011518045.1:c.3313C>A	XP_011516347.1:p.Pro1105Thr
XM_011518046.1:c.3475C>A	XP_011516348.1:p.Pro1159Thr
XM_011518047.1:c.3409C>A	XP_011516349.1:p.Pro1137Thr
XM_011518048.1:c.3409C>A	XP_011516350.1:p.Pro1137Thr
XM_011518049.1:c.1849C>A	XP_011516351.1:p.Pro617Thr
XM_011518045.3:c.3313C>A	XP_011516347.1:p.Pro1105Thr
XM_011518046.2:c.3475C>A	XP_011516348.1:p.Pro1159Thr
XM_011518047.3:c.3409C>A	XP_011516349.1:p.Pro1137Thr
XM_011518048.2:c.3409C>A	XP_011516350.1:p.Pro1137Thr
XM_011518049.2:c.1849C>A	XP_011516351.1:p.Pro617Thr
XM_017015173.1:c.3409C>A	XP_016870662.1:p.Pro1137Thr
XM_017015174.1:c.3475C>A	XP_016870663.1:p.Pro1159Thr
NM_001190458.2:c.3313C>A	NP_001177387.1:p.Pro1105Thr
NM_001193536.2:c.3409C>A	NP_001180465.1:p.Pro1137Thr
NM_203447.4:c.3613C>A MANE Select	NP_982272.2:p.Pro1205Thr