Canonical Allele Identifier: CA404105737
Gene: DOCK6 HGNC NCBI
ANGPTL8 HGNC NCBI

Linked Data

dbSNP Id: rs1439436787

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11239919C>G , CM000681.2:g.11239919C>G GRCh38
NC_000019.9:g.11350595C>G , CM000681.1:g.11350595C>G GRCh37
NC_000019.8:g.11211595C>G NCBI36
NG_031953.1:g.27574G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.1644-1615G>C (DOCK6) ENSP00000468638.2:n.1644-1615G>C
ENST00000294618.12:c.1644-1615G>C (DOCK6) MANE Select ENSP00000294618.6:n.1644-1615G>C
ENST00000252453.12:c.282C>G (ANGPTL8) MANE Select ENSP00000252453.7:p.Ser94Arg
ENST00000294618.11:c.1644-1615G>C (DOCK6) ENSP00000294618.6:n.1644-1615G>C
ENST00000587543.1:c.23C>G (ANGPTL8)
ENST00000591200.5:c.1-216C>G (ANGPTL8) ENSP00000464941.1:n.1-216C>G
ENST00000616433.4:c.282C>G (ANGPTL8) ENSP00000479969.1:p.Ser94Arg
NM_018687.6:c.282C>G (ANGPTL8) NP_061157.3:p.Ser94Arg
NM_020812.3:c.1644-1615G>C (DOCK6) NP_065863.2:n.1644-1615G>C
XM_005260000.2:c.1644-1615G>C (DOCK6) XP_005260057.1:n.1644-1615G>C
XM_005260001.2:c.1644-1615G>C (DOCK6) XP_005260058.1:n.1644-1615G>C
XM_011528150.1:c.1677-1615G>C (DOCK6) XP_011526452.1:n.1677-1615G>C
XM_011528151.1:c.1677-1615G>C (DOCK6) XP_011526453.1:n.1677-1615G>C
XM_011528152.1:c.1677-1615G>C (DOCK6) XP_011526454.1:n.1677-1615G>C
XM_011528153.1:c.1677-1615G>C (DOCK6) XP_011526455.1:n.1677-1615G>C
XR_936195.1:n.1738-1615G>C (DOCK6)
XR_936196.1:n.1738-1615G>C (DOCK6)
XR_936197.1:n.1738-1615G>C (DOCK6)
XR_936198.1:n.1738-1615G>C (DOCK6)
NM_001367830.1:c.1644-1615G>C (DOCK6) NP_001354759.1:n.1644-1615G>C
NM_018687.7:c.282C>G (ANGPTL8) MANE Select NP_061157.3:p.Ser94Arg
NM_020812.4:c.1644-1615G>C (DOCK6) MANE Select NP_065863.2:n.1644-1615G>C