Canonical Allele Identifier: CA404069669

Gene: DOCK6

Linked Data

• dbSNP Id: rs201387914
• gnomAD v2: 19-11311390-A-C
• gnomAD v4: 19-11200714-A-C
• MyVariant Identifiers: chr19:g.11311390A>C (hg19) ; chr19:g.11200714A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11200714A>C , CM000681.2:g.11200714A>C	GRCh38
NC_000019.9:g.11311390A>C , CM000681.1:g.11311390A>C	GRCh37
NC_000019.8:g.11172390A>C	NCBI36
NG_031953.1:g.66779T>G
NG_051186.1:g.1854T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000587656.6:c.6044+2T>G	ENSP00000468638.2:n.6044+2T>G
ENST00000294618.12:c.5939+2T>G MANE Select	ENSP00000294618.6:n.5939+2T>G
ENST00000294618.11:c.5939+2T>G	ENSP00000294618.6:n.5939+2T>G
ENST00000586702.1:n.842+2T>G
ENST00000587656.5:c.3804+2T>G
ENST00000587734.1:c.76-1175T>G	ENSP00000468291.1:n.76-1175T>G
NM_020812.3:c.5939+2T>G	NP_065863.2:n.5939+2T>G
XM_005260000.2:c.6137+2T>G	XP_005260057.1:n.6137+2T>G
XM_005260001.2:c.6044+2T>G	XP_005260058.1:n.6044+2T>G
XM_006722804.2:c.3275+2T>G	XP_006722867.1:n.3275+2T>G
XM_011528150.1:c.6077+2T>G	XP_011526452.1:n.6077+2T>G
XM_011528151.1:c.6065+2T>G	XP_011526453.1:n.6065+2T>G
XM_011528152.1:c.5972+2T>G	XP_011526454.1:n.5972+2T>G
XR_936195.1:n.6184+2T>G
XM_006722804.3:c.3275+2T>G	XP_006722867.1:n.3275+2T>G
NM_001367830.1:c.6044+2T>G	NP_001354759.1:n.6044+2T>G
NM_020812.4:c.5939+2T>G MANE Select	NP_065863.2:n.5939+2T>G