Canonical Allele Identifier: CA993518943
Gene: DOCK6 HGNC NCBI

Linked Data

dbSNP Id: rs2079558888

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11220189G>A , CM000681.2:g.11220189G>A GRCh38
NC_000019.9:g.11330865G>A , CM000681.1:g.11330865G>A GRCh37
NC_000019.8:g.11191865G>A NCBI36
NG_031953.1:g.47304C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000587656.6:c.3655+1662C>T ENSP00000468638.2:n.3655+1662C>T
ENST00000294618.12:c.3550+1662C>T MANE Select ENSP00000294618.6:n.3550+1662C>T
ENST00000294618.11:c.3550+1662C>T ENSP00000294618.6:n.3550+1662C>T
ENST00000587656.5:c.1415+1662C>T
NM_020812.3:c.3550+1662C>T NP_065863.2:n.3550+1662C>T
XM_005260000.2:c.3748+1662C>T XP_005260057.1:n.3748+1662C>T
XM_005260001.2:c.3655+1662C>T XP_005260058.1:n.3655+1662C>T
XM_006722804.2:c.886+1662C>T XP_006722867.1:n.886+1662C>T
XM_011528150.1:c.3688+1662C>T XP_011526452.1:n.3688+1662C>T
XM_011528151.1:c.3676+1662C>T XP_011526453.1:n.3676+1662C>T
XM_011528152.1:c.3583+1662C>T XP_011526454.1:n.3583+1662C>T
XM_011528153.1:c.3688+1662C>T XP_011526455.1:n.3688+1662C>T
XR_936195.1:n.3749+1662C>T
XR_936196.1:n.3766+1662C>T
XM_006722804.3:c.886+1662C>T XP_006722867.1:n.886+1662C>T
NM_001367830.1:c.3655+1662C>T NP_001354759.1:n.3655+1662C>T
NM_020812.4:c.3550+1662C>T MANE Select NP_065863.2:n.3550+1662C>T