Canonical Allele Identifier: CA404069753

Gene: DOCK6

Linked Data

• MyVariant Identifiers: chr19:g.11311402A>G (hg19) ; chr19:g.11200726A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200726A>G , CM000681.2:g.11200726A>G	GRCh38
NC_000019.9:g.11311402A>G , CM000681.1:g.11311402A>G	GRCh37
NC_000019.8:g.11172402A>G	NCBI36
NG_031953.1:g.66767T>C
NG_051186.1:g.1842T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6034T>C	ENSP00000468638.2:p.Phe2012Leu
ENST00000294618.12:c.5929T>C MANE Select	ENSP00000294618.6:p.Phe1977Leu
ENST00000294618.11:c.5929T>C	ENSP00000294618.6:p.Phe1977Leu
ENST00000586702.1:n.832T>C
ENST00000587656.5:c.3794T>C
ENST00000587734.1:c.75+1163T>C	ENSP00000468291.1:n.75+1163T>C
NM_020812.3:c.5929T>C	NP_065863.2:p.Phe1977Leu
XM_005260000.2:c.6127T>C	XP_005260057.1:p.Phe2043Leu
XM_005260001.2:c.6034T>C	XP_005260058.1:p.Phe2012Leu
XM_006722804.2:c.3265T>C	XP_006722867.1:p.Phe1089Leu
XM_011528150.1:c.6067T>C	XP_011526452.1:p.Phe2023Leu
XM_011528151.1:c.6055T>C	XP_011526453.1:p.Phe2019Leu
XM_011528152.1:c.5962T>C	XP_011526454.1:p.Phe1988Leu
XR_936195.1:n.6174T>C
XM_006722804.3:c.3265T>C	XP_006722867.1:p.Phe1089Leu
NM_001367830.1:c.6034T>C	NP_001354759.1:p.Phe2012Leu
NM_020812.4:c.5929T>C MANE Select	NP_065863.2:p.Phe1977Leu