Canonical Allele Identifier: CA2322832006

Gene: DOCK6

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232232C= , CM000681.2:g.11232232C=	GRCh38
NC_000019.9:g.11342908C= , CM000681.1:g.11342908C=	GRCh37
NC_000019.8:g.11203908C=	NCBI36
NG_031953.1:g.35261G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2776G=	ENSP00000468638.2:p.Ala926=
ENST00000294618.12:c.2718+971G= MANE Select	ENSP00000294618.6:n.2718+971G=
ENST00000294618.11:c.2718+971G=	ENSP00000294618.6:n.2718+971G=
ENST00000585904.1:c.379G=	ENSP00000465767.1:p.Ala127=
ENST00000587656.5:c.536G=
ENST00000590680.5:c.1061+971G=
NM_020812.3:c.2718+971G=	NP_065863.2:n.2718+971G=
XM_005260000.2:c.2776G=	XP_005260057.1:p.Ala926=
XM_005260001.2:c.2776G=	XP_005260058.1:p.Ala926=
XM_006722804.2:c.54+807G=	XP_006722867.1:n.54+807G=
XM_011528150.1:c.2809G=	XP_011526452.1:p.Ala937=
XM_011528151.1:c.2751+971G=	XP_011526453.1:n.2751+971G=
XM_011528152.1:c.2751+971G=	XP_011526454.1:n.2751+971G=
XM_011528153.1:c.2809G=	XP_011526455.1:p.Ala937=
XR_936195.1:n.2870G=
XR_936196.1:n.2812+971G=
XR_936197.1:n.2870G=
XR_936198.1:n.2812+971G=
XM_006722804.3:c.54+807G=	XP_006722867.1:n.54+807G=
NM_001367830.1:c.2776G=	NP_001354759.1:p.Ala926=
NM_020812.4:c.2718+971G= MANE Select	NP_065863.2:n.2718+971G=