Canonical Allele Identifier: CA404094624

Gene: DOCK6

Linked Data

• MyVariant Identifiers: chr19:g.11342953A>G (hg19) ; chr19:g.11232277A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232277A>G , CM000681.2:g.11232277A>G	GRCh38
NC_000019.9:g.11342953A>G , CM000681.1:g.11342953A>G	GRCh37
NC_000019.8:g.11203953A>G	NCBI36
NG_031953.1:g.35216T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2731T>C	ENSP00000468638.2:p.Ser911Pro
ENST00000294618.12:c.2718+926T>C MANE Select	ENSP00000294618.6:n.2718+926T>C
ENST00000294618.11:c.2718+926T>C	ENSP00000294618.6:n.2718+926T>C
ENST00000585904.1:c.334T>C	ENSP00000465767.1:p.Ser112Pro
ENST00000587656.5:c.491T>C
ENST00000590680.5:c.1061+926T>C
NM_020812.3:c.2718+926T>C	NP_065863.2:n.2718+926T>C
XM_005260000.2:c.2731T>C	XP_005260057.1:p.Ser911Pro
XM_005260001.2:c.2731T>C	XP_005260058.1:p.Ser911Pro
XM_006722804.2:c.54+762T>C	XP_006722867.1:n.54+762T>C
XM_011528150.1:c.2764T>C	XP_011526452.1:p.Ser922Pro
XM_011528151.1:c.2751+926T>C	XP_011526453.1:n.2751+926T>C
XM_011528152.1:c.2751+926T>C	XP_011526454.1:n.2751+926T>C
XM_011528153.1:c.2764T>C	XP_011526455.1:p.Ser922Pro
XR_936195.1:n.2825T>C
XR_936196.1:n.2812+926T>C
XR_936197.1:n.2825T>C
XR_936198.1:n.2812+926T>C
XM_006722804.3:c.54+762T>C	XP_006722867.1:n.54+762T>C
NM_001367830.1:c.2731T>C	NP_001354759.1:p.Ser911Pro
NM_020812.4:c.2718+926T>C MANE Select	NP_065863.2:n.2718+926T>C