Canonical Allele Identifier: CA404069688

Gene: DOCK6

Linked Data

• MyVariant Identifiers: chr19:g.11311392T>G (hg19) ; chr19:g.11200716T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200716T>G , CM000681.2:g.11200716T>G	GRCh38
NC_000019.9:g.11311392T>G , CM000681.1:g.11311392T>G	GRCh37
NC_000019.8:g.11172392T>G	NCBI36
NG_031953.1:g.66777A>C
NG_051186.1:g.1852A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6044A>C	ENSP00000468638.2:p.Lys2015Thr
ENST00000294618.12:c.5939A>C MANE Select	ENSP00000294618.6:p.Lys1980Thr
ENST00000294618.11:c.5939A>C	ENSP00000294618.6:p.Lys1980Thr
ENST00000586702.1:n.842A>C
ENST00000587656.5:c.3804A>C
ENST00000587734.1:c.75+1173A>C	ENSP00000468291.1:n.75+1173A>C
NM_020812.3:c.5939A>C	NP_065863.2:p.Lys1980Thr
XM_005260000.2:c.6137A>C	XP_005260057.1:p.Lys2046Thr
XM_005260001.2:c.6044A>C	XP_005260058.1:p.Lys2015Thr
XM_006722804.2:c.3275A>C	XP_006722867.1:p.Lys1092Thr
XM_011528150.1:c.6077A>C	XP_011526452.1:p.Lys2026Thr
XM_011528151.1:c.6065A>C	XP_011526453.1:p.Lys2022Thr
XM_011528152.1:c.5972A>C	XP_011526454.1:p.Lys1991Thr
XR_936195.1:n.6184A>C
XM_006722804.3:c.3275A>C	XP_006722867.1:p.Lys1092Thr
NM_001367830.1:c.6044A>C	NP_001354759.1:p.Lys2015Thr
NM_020812.4:c.5939A>C MANE Select	NP_065863.2:p.Lys1980Thr