Canonical Allele Identifier: CA505745656

Gene: DOCK6

Linked Data

• dbSNP Id: rs2079154846
• gnomAD v4: 19-11200718-C-T
• MyVariant Identifiers: chr19:g.11311394C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200718C>T , CM000681.2:g.11200718C>T	GRCh38
NC_000019.9:g.11311394C>T , CM000681.1:g.11311394C>T	GRCh37
NC_000019.8:g.11172394C>T	NCBI36
NG_031953.1:g.66775G>A
NG_051186.1:g.1850G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6042G>A	ENSP00000468638.2:p.Lys2014=
ENST00000294618.12:c.5937G>A MANE Select	ENSP00000294618.6:p.Lys1979=
ENST00000294618.11:c.5937G>A	ENSP00000294618.6:p.Lys1979=
ENST00000586702.1:n.840G>A
ENST00000587656.5:c.3802G>A
ENST00000587734.1:c.75+1171G>A	ENSP00000468291.1:n.75+1171G>A
NM_020812.3:c.5937G>A	NP_065863.2:p.Lys1979=
XM_005260000.2:c.6135G>A	XP_005260057.1:p.Lys2045=
XM_005260001.2:c.6042G>A	XP_005260058.1:p.Lys2014=
XM_006722804.2:c.3273G>A	XP_006722867.1:p.Lys1091=
XM_011528150.1:c.6075G>A	XP_011526452.1:p.Lys2025=
XM_011528151.1:c.6063G>A	XP_011526453.1:p.Lys2021=
XM_011528152.1:c.5970G>A	XP_011526454.1:p.Lys1990=
XR_936195.1:n.6182G>A
XM_006722804.3:c.3273G>A	XP_006722867.1:p.Lys1091=
NM_001367830.1:c.6042G>A	NP_001354759.1:p.Lys2014=
NM_020812.4:c.5937G>A MANE Select	NP_065863.2:p.Lys1979=