Canonical Allele Identifier: CA404069695

Gene: DOCK6

Linked Data

• MyVariant Identifiers: chr19:g.11311393T>A (hg19) ; chr19:g.11200717T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200717T>A , CM000681.2:g.11200717T>A	GRCh38
NC_000019.9:g.11311393T>A , CM000681.1:g.11311393T>A	GRCh37
NC_000019.8:g.11172393T>A	NCBI36
NG_031953.1:g.66776A>T
NG_051186.1:g.1851A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6043A>T	ENSP00000468638.2:p.Lys2015Ter
ENST00000294618.12:c.5938A>T MANE Select	ENSP00000294618.6:p.Lys1980Ter
ENST00000294618.11:c.5938A>T	ENSP00000294618.6:p.Lys1980Ter
ENST00000586702.1:n.841A>T
ENST00000587656.5:c.3803A>T
ENST00000587734.1:c.75+1172A>T	ENSP00000468291.1:n.75+1172A>T
NM_020812.3:c.5938A>T	NP_065863.2:p.Lys1980Ter
XM_005260000.2:c.6136A>T	XP_005260057.1:p.Lys2046Ter
XM_005260001.2:c.6043A>T	XP_005260058.1:p.Lys2015Ter
XM_006722804.2:c.3274A>T	XP_006722867.1:p.Lys1092Ter
XM_011528150.1:c.6076A>T	XP_011526452.1:p.Lys2026Ter
XM_011528151.1:c.6064A>T	XP_011526453.1:p.Lys2022Ter
XM_011528152.1:c.5971A>T	XP_011526454.1:p.Lys1991Ter
XR_936195.1:n.6183A>T
XM_006722804.3:c.3274A>T	XP_006722867.1:p.Lys1092Ter
NM_001367830.1:c.6043A>T	NP_001354759.1:p.Lys2015Ter
NM_020812.4:c.5938A>T MANE Select	NP_065863.2:p.Lys1980Ter