Canonical Allele Identifier: CA404094490

Gene: DOCK6

Linked Data

• MyVariant Identifiers: chr19:g.11342887G>C (hg19) ; chr19:g.11232211G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11232211G>C , CM000681.2:g.11232211G>C	GRCh38
NC_000019.9:g.11342887G>C , CM000681.1:g.11342887G>C	GRCh37
NC_000019.8:g.11203887G>C	NCBI36
NG_031953.1:g.35282C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587656.6:c.2797C>G	ENSP00000468638.2:p.Pro933Ala
ENST00000294618.12:c.2718+992C>G MANE Select	ENSP00000294618.6:n.2718+992C>G
ENST00000294618.11:c.2718+992C>G	ENSP00000294618.6:n.2718+992C>G
ENST00000585904.1:c.400C>G	ENSP00000465767.1:p.Pro134Ala
ENST00000587656.5:c.557C>G
ENST00000590680.5:c.1061+992C>G
NM_020812.3:c.2718+992C>G	NP_065863.2:n.2718+992C>G
XM_005260000.2:c.2797C>G	XP_005260057.1:p.Pro933Ala
XM_005260001.2:c.2797C>G	XP_005260058.1:p.Pro933Ala
XM_006722804.2:c.54+828C>G	XP_006722867.1:n.54+828C>G
XM_011528150.1:c.2830C>G	XP_011526452.1:p.Pro944Ala
XM_011528151.1:c.2751+992C>G	XP_011526453.1:n.2751+992C>G
XM_011528152.1:c.2751+992C>G	XP_011526454.1:n.2751+992C>G
XM_011528153.1:c.2830C>G	XP_011526455.1:p.Pro944Ala
XR_936195.1:n.2891C>G
XR_936196.1:n.2812+992C>G
XR_936197.1:n.2891C>G
XR_936198.1:n.2812+992C>G
XM_006722804.3:c.54+828C>G	XP_006722867.1:n.54+828C>G
NM_001367830.1:c.2797C>G	NP_001354759.1:p.Pro933Ala
NM_020812.4:c.2718+992C>G MANE Select	NP_065863.2:n.2718+992C>G