Canonical Allele Identifier: CA505745664

Gene: DOCK6

Linked Data

• MyVariant Identifiers: chr19:g.11311400G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200724G>A , CM000681.2:g.11200724G>A	GRCh38
NC_000019.9:g.11311400G>A , CM000681.1:g.11311400G>A	GRCh37
NC_000019.8:g.11172400G>A	NCBI36
NG_031953.1:g.66769C>T
NG_051186.1:g.1844C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6036C>T	ENSP00000468638.2:p.Phe2012=
ENST00000294618.12:c.5931C>T MANE Select	ENSP00000294618.6:p.Phe1977=
ENST00000294618.11:c.5931C>T	ENSP00000294618.6:p.Phe1977=
ENST00000586702.1:n.834C>T
ENST00000587656.5:c.3796C>T
ENST00000587734.1:c.75+1165C>T	ENSP00000468291.1:n.75+1165C>T
NM_020812.3:c.5931C>T	NP_065863.2:p.Phe1977=
XM_005260000.2:c.6129C>T	XP_005260057.1:p.Phe2043=
XM_005260001.2:c.6036C>T	XP_005260058.1:p.Phe2012=
XM_006722804.2:c.3267C>T	XP_006722867.1:p.Phe1089=
XM_011528150.1:c.6069C>T	XP_011526452.1:p.Phe2023=
XM_011528151.1:c.6057C>T	XP_011526453.1:p.Phe2019=
XM_011528152.1:c.5964C>T	XP_011526454.1:p.Phe1988=
XR_936195.1:n.6176C>T
XM_006722804.3:c.3267C>T	XP_006722867.1:p.Phe1089=
NM_001367830.1:c.6036C>T	NP_001354759.1:p.Phe2012=
NM_020812.4:c.5931C>T MANE Select	NP_065863.2:p.Phe1977=