Canonical Allele Identifier: CA14737907

Gene: DOCK6 DOCK6-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11214214T>C , CM000681.2:g.11214214T>C	GRCh38
NC_000019.9:g.11324890T>C , CM000681.1:g.11324890T>C	GRCh37
NC_000019.8:g.11185890T>C	NCBI36
NG_031953.1:g.53279A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020812.4:c.4338+61A>G (DOCK6) MANE Select	NP_065863.2:n.4338+61A>G
ENST00000294618.12:c.4338+61A>G (DOCK6) MANE Select	ENSP00000294618.6:n.4338+61A>G
NM_001367830.1:c.4443+61A>G (DOCK6)	NP_001354759.1:n.4443+61A>G
NM_020812.3:c.4338+61A>G (DOCK6)	NP_065863.2:n.4338+61A>G
NR_134909.1:n.538-1923T>C (DOCK6-AS1)
ENST00000294618.11:c.4338+61A>G (DOCK6)	ENSP00000294618.6:n.4338+61A>G
ENST00000587656.5:c.2203+61A>G (DOCK6)
ENST00000587656.6:c.4443+61A>G (DOCK6)	ENSP00000468638.2:n.4443+61A>G
XM_005260000.2:c.4536+61A>G (DOCK6)	XP_005260057.1:n.4536+61A>G
XM_005260001.2:c.4443+61A>G (DOCK6)	XP_005260058.1:n.4443+61A>G
XM_006722804.2:c.1674+61A>G (DOCK6)	XP_006722867.1:n.1674+61A>G
XM_006722804.3:c.1674+61A>G (DOCK6)	XP_006722867.1:n.1674+61A>G
XM_011528150.1:c.4476+61A>G (DOCK6)	XP_011526452.1:n.4476+61A>G
XM_011528151.1:c.4464+61A>G (DOCK6)	XP_011526453.1:n.4464+61A>G
XM_011528152.1:c.4371+61A>G (DOCK6)	XP_011526454.1:n.4371+61A>G
XR_936195.1:n.4537+61A>G (DOCK6)
XR_936315.1:n.538-1923T>C (DOCK6-AS1)