Canonical Allele Identifier: CA2322832005

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232231G= , CM000681.2:g.11232231G=	GRCh38
NC_000019.9:g.11342907G= , CM000681.1:g.11342907G=	GRCh37
NC_000019.8:g.11203907G=	NCBI36
NG_031953.1:g.35262C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2777C=	ENSP00000468638.2:p.Ala926=
ENST00000294618.12:c.2718+972C= MANE Select	ENSP00000294618.6:n.2718+972C=
ENST00000294618.11:c.2718+972C=	ENSP00000294618.6:n.2718+972C=
ENST00000585904.1:c.380C=	ENSP00000465767.1:p.Ala127=
ENST00000587656.5:c.537C=
ENST00000590680.5:c.1061+972C=
NM_020812.3:c.2718+972C=	NP_065863.2:n.2718+972C=
XM_005260000.2:c.2777C=	XP_005260057.1:p.Ala926=
XM_005260001.2:c.2777C=	XP_005260058.1:p.Ala926=
XM_006722804.2:c.54+808C=	XP_006722867.1:n.54+808C=
XM_011528150.1:c.2810C=	XP_011526452.1:p.Ala937=
XM_011528151.1:c.2751+972C=	XP_011526453.1:n.2751+972C=
XM_011528152.1:c.2751+972C=	XP_011526454.1:n.2751+972C=
XM_011528153.1:c.2810C=	XP_011526455.1:p.Ala937=
XR_936195.1:n.2871C=
XR_936196.1:n.2812+972C=
XR_936197.1:n.2871C=
XR_936198.1:n.2812+972C=
XM_006722804.3:c.54+808C=	XP_006722867.1:n.54+808C=
NM_001367830.1:c.2777C=	NP_001354759.1:p.Ala926=
NM_020812.4:c.2718+972C= MANE Select	NP_065863.2:n.2718+972C=