Canonical Allele Identifier: CA404094613

Gene: DOCK6

Linked Data

• MyVariant Identifiers: chr19:g.11342948G>C (hg19) ; chr19:g.11232272G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232272G>C , CM000681.2:g.11232272G>C	GRCh38
NC_000019.9:g.11342948G>C , CM000681.1:g.11342948G>C	GRCh37
NC_000019.8:g.11203948G>C	NCBI36
NG_031953.1:g.35221C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2736C>G	ENSP00000468638.2:p.His912Gln
ENST00000294618.12:c.2718+931C>G MANE Select	ENSP00000294618.6:n.2718+931C>G
ENST00000294618.11:c.2718+931C>G	ENSP00000294618.6:n.2718+931C>G
ENST00000585904.1:c.339C>G	ENSP00000465767.1:p.His113Gln
ENST00000587656.5:c.496C>G
ENST00000590680.5:c.1061+931C>G
NM_020812.3:c.2718+931C>G	NP_065863.2:n.2718+931C>G
XM_005260000.2:c.2736C>G	XP_005260057.1:p.His912Gln
XM_005260001.2:c.2736C>G	XP_005260058.1:p.His912Gln
XM_006722804.2:c.54+767C>G	XP_006722867.1:n.54+767C>G
XM_011528150.1:c.2769C>G	XP_011526452.1:p.His923Gln
XM_011528151.1:c.2751+931C>G	XP_011526453.1:n.2751+931C>G
XM_011528152.1:c.2751+931C>G	XP_011526454.1:n.2751+931C>G
XM_011528153.1:c.2769C>G	XP_011526455.1:p.His923Gln
XR_936195.1:n.2830C>G
XR_936196.1:n.2812+931C>G
XR_936197.1:n.2830C>G
XR_936198.1:n.2812+931C>G
XM_006722804.3:c.54+767C>G	XP_006722867.1:n.54+767C>G
NM_001367830.1:c.2736C>G	NP_001354759.1:p.His912Gln
NM_020812.4:c.2718+931C>G MANE Select	NP_065863.2:n.2718+931C>G