Canonical Allele Identifier: CA404105790
Gene: DOCK6 HGNC NCBI
ANGPTL8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11239928G>C , CM000681.2:g.11239928G>C GRCh38
NC_000019.9:g.11350604G>C , CM000681.1:g.11350604G>C GRCh37
NC_000019.8:g.11211604G>C NCBI36
NG_031953.1:g.27565C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.1644-1624C>G (DOCK6) ENSP00000468638.2:n.1644-1624C>G
ENST00000294618.12:c.1644-1624C>G (DOCK6) MANE Select ENSP00000294618.6:n.1644-1624C>G
ENST00000252453.12:c.291G>C (ANGPTL8) MANE Select ENSP00000252453.7:p.Glu97Asp
ENST00000294618.11:c.1644-1624C>G (DOCK6) ENSP00000294618.6:n.1644-1624C>G
ENST00000587543.1:c.32G>C (ANGPTL8)
ENST00000591200.5:c.1-207G>C (ANGPTL8) ENSP00000464941.1:n.1-207G>C
ENST00000616433.4:c.291G>C (ANGPTL8) ENSP00000479969.1:p.Glu97Asp
NM_018687.6:c.291G>C (ANGPTL8) NP_061157.3:p.Glu97Asp
NM_020812.3:c.1644-1624C>G (DOCK6) NP_065863.2:n.1644-1624C>G
XM_005260000.2:c.1644-1624C>G (DOCK6) XP_005260057.1:n.1644-1624C>G
XM_005260001.2:c.1644-1624C>G (DOCK6) XP_005260058.1:n.1644-1624C>G
XM_011528150.1:c.1677-1624C>G (DOCK6) XP_011526452.1:n.1677-1624C>G
XM_011528151.1:c.1677-1624C>G (DOCK6) XP_011526453.1:n.1677-1624C>G
XM_011528152.1:c.1677-1624C>G (DOCK6) XP_011526454.1:n.1677-1624C>G
XM_011528153.1:c.1677-1624C>G (DOCK6) XP_011526455.1:n.1677-1624C>G
XR_936195.1:n.1738-1624C>G (DOCK6)
XR_936196.1:n.1738-1624C>G (DOCK6)
XR_936197.1:n.1738-1624C>G (DOCK6)
XR_936198.1:n.1738-1624C>G (DOCK6)
NM_001367830.1:c.1644-1624C>G (DOCK6) NP_001354759.1:n.1644-1624C>G
NM_018687.7:c.291G>C (ANGPTL8) MANE Select NP_061157.3:p.Glu97Asp
NM_020812.4:c.1644-1624C>G (DOCK6) MANE Select NP_065863.2:n.1644-1624C>G