Canonical Allele Identifier: CA404069733

Gene: DOCK6

Linked Data

• MyVariant Identifiers: chr19:g.11311399A>T (hg19) ; chr19:g.11200723A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200723A>T , CM000681.2:g.11200723A>T	GRCh38
NC_000019.9:g.11311399A>T , CM000681.1:g.11311399A>T	GRCh37
NC_000019.8:g.11172399A>T	NCBI36
NG_031953.1:g.66770T>A
NG_051186.1:g.1845T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6037T>A	ENSP00000468638.2:p.Cys2013Ser
ENST00000294618.12:c.5932T>A MANE Select	ENSP00000294618.6:p.Cys1978Ser
ENST00000294618.11:c.5932T>A	ENSP00000294618.6:p.Cys1978Ser
ENST00000586702.1:n.835T>A
ENST00000587656.5:c.3797T>A
ENST00000587734.1:c.75+1166T>A	ENSP00000468291.1:n.75+1166T>A
NM_020812.3:c.5932T>A	NP_065863.2:p.Cys1978Ser
XM_005260000.2:c.6130T>A	XP_005260057.1:p.Cys2044Ser
XM_005260001.2:c.6037T>A	XP_005260058.1:p.Cys2013Ser
XM_006722804.2:c.3268T>A	XP_006722867.1:p.Cys1090Ser
XM_011528150.1:c.6070T>A	XP_011526452.1:p.Cys2024Ser
XM_011528151.1:c.6058T>A	XP_011526453.1:p.Cys2020Ser
XM_011528152.1:c.5965T>A	XP_011526454.1:p.Cys1989Ser
XR_936195.1:n.6177T>A
XM_006722804.3:c.3268T>A	XP_006722867.1:p.Cys1090Ser
NM_001367830.1:c.6037T>A	NP_001354759.1:p.Cys2013Ser
NM_020812.4:c.5932T>A MANE Select	NP_065863.2:p.Cys1978Ser