Canonical Allele Identifier: CA404094520

Gene: DOCK6

Linked Data

• MyVariant Identifiers: chr19:g.11342905C>T (hg19) ; chr19:g.11232229C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232229C>T , CM000681.2:g.11232229C>T	GRCh38
NC_000019.9:g.11342905C>T , CM000681.1:g.11342905C>T	GRCh37
NC_000019.8:g.11203905C>T	NCBI36
NG_031953.1:g.35264G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2779G>A	ENSP00000468638.2:p.Val927Met
ENST00000294618.12:c.2718+974G>A MANE Select	ENSP00000294618.6:n.2718+974G>A
ENST00000294618.11:c.2718+974G>A	ENSP00000294618.6:n.2718+974G>A
ENST00000585904.1:c.382G>A	ENSP00000465767.1:p.Val128Met
ENST00000587656.5:c.539G>A
ENST00000590680.5:c.1061+974G>A
NM_020812.3:c.2718+974G>A	NP_065863.2:n.2718+974G>A
XM_005260000.2:c.2779G>A	XP_005260057.1:p.Val927Met
XM_005260001.2:c.2779G>A	XP_005260058.1:p.Val927Met
XM_006722804.2:c.54+810G>A	XP_006722867.1:n.54+810G>A
XM_011528150.1:c.2812G>A	XP_011526452.1:p.Val938Met
XM_011528151.1:c.2751+974G>A	XP_011526453.1:n.2751+974G>A
XM_011528152.1:c.2751+974G>A	XP_011526454.1:n.2751+974G>A
XM_011528153.1:c.2812G>A	XP_011526455.1:p.Val938Met
XR_936195.1:n.2873G>A
XR_936196.1:n.2812+974G>A
XR_936197.1:n.2873G>A
XR_936198.1:n.2812+974G>A
XM_006722804.3:c.54+810G>A	XP_006722867.1:n.54+810G>A
NM_001367830.1:c.2779G>A	NP_001354759.1:p.Val927Met
NM_020812.4:c.2718+974G>A MANE Select	NP_065863.2:n.2718+974G>A