Canonical Allele Identifier: CA463699931

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.441369A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.441369A>C , CM000671.2:g.441369A>C	GRCh38
NC_000009.11:g.441369A>C , CM000671.1:g.441369A>C	GRCh37
NC_000009.10:g.431369A>C	NCBI36
NG_017007.1:g.231505A>C , LRG_196:g.231505A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.5007A>C	ENSP00000371766.2:p.Thr1669=
ENST00000683406.1:n.1782A>C
ENST00000684637.1:n.988A>C
ENST00000685949.1:n.4095A>C
ENST00000432829.7:c.5307A>C MANE Select	ENSP00000394888.3:p.Thr1769=
ENST00000382329.1:c.3708A>C	ENSP00000371766.1:p.Thr1236=
ENST00000432829.6:c.5307A>C	ENSP00000394888.3:p.Thr1769=
ENST00000453981.5:c.5103A>C	ENSP00000408464.2:p.Thr1701=
ENST00000469391.5:c.5007A>C	ENSP00000419438.1:p.Thr1669=
ENST00000495184.5:n.7262A>C
NM_001190458.1:c.5007A>C	NP_001177387.1:p.Thr1669=
NM_001193536.1:c.5103A>C	NP_001180465.1:p.Thr1701=
NM_203447.3:c.5307A>C , LRG_196t1:c.5307A>C	NP_982272.2:p.Thr1769=
XM_011518045.1:c.5007A>C	XP_011516347.1:p.Thr1669=
XM_011518046.1:c.5169A>C	XP_011516348.1:p.Thr1723=
XM_011518047.1:c.5103A>C	XP_011516349.1:p.Thr1701=
XM_011518048.1:c.5103A>C	XP_011516350.1:p.Thr1701=
XM_011518049.1:c.3543A>C	XP_011516351.1:p.Thr1181=
XM_011518045.3:c.5007A>C	XP_011516347.1:p.Thr1669=
XM_011518046.2:c.5169A>C	XP_011516348.1:p.Thr1723=
XM_011518047.3:c.5103A>C	XP_011516349.1:p.Thr1701=
XM_011518048.2:c.5103A>C	XP_011516350.1:p.Thr1701=
XM_011518049.2:c.3543A>C	XP_011516351.1:p.Thr1181=
XM_017015173.1:c.5103A>C	XP_016870662.1:p.Thr1701=
XM_017015174.1:c.5169A>C	XP_016870663.1:p.Thr1723=
NM_001190458.2:c.5007A>C	NP_001177387.1:p.Thr1669=
NM_001193536.2:c.5103A>C	NP_001180465.1:p.Thr1701=
NM_203447.4:c.5307A>C MANE Select	NP_982272.2:p.Thr1769=