Canonical Allele Identifier: CA305301733

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200310G>C , CM000681.2:g.11200310G>C	GRCh38
NC_000019.9:g.11310986G>C , CM000681.1:g.11310986G>C	GRCh37
NC_000019.8:g.11171986G>C	NCBI36
NG_031953.1:g.67183C>G
NG_051186.1:g.2258C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.6204C>G	ENSP00000468638.2:p.Leu2068=
ENST00000294618.12:c.6099C>G MANE Select	ENSP00000294618.6:p.Leu2033=
ENST00000294618.11:c.6099C>G	ENSP00000294618.6:p.Leu2033=
ENST00000586702.1:n.1002C>G
ENST00000587656.5:c.3964C>G
ENST00000587734.1:c.76-771C>G	ENSP00000468291.1:n.76-771C>G
NM_020812.3:c.6099C>G	NP_065863.2:p.Leu2033=
XM_005260000.2:c.6297C>G	XP_005260057.1:p.Leu2099=
XM_005260001.2:c.6204C>G	XP_005260058.1:p.Leu2068=
XM_006722804.2:c.3435C>G	XP_006722867.1:p.Leu1145=
XM_011528150.1:c.6237C>G	XP_011526452.1:p.Leu2079=
XM_011528151.1:c.6225C>G	XP_011526453.1:p.Leu2075=
XM_011528152.1:c.6132C>G	XP_011526454.1:p.Leu2044=
XM_006722804.3:c.3435C>G	XP_006722867.1:p.Leu1145=
NM_001367830.1:c.6204C>G	NP_001354759.1:p.Leu2068=
NM_020812.4:c.6099C>G MANE Select	NP_065863.2:p.Leu2033=