Canonical Allele Identifier: CA372763135

Gene: DOCK8

Linked Data

• gnomAD v4: 9-377032-C-G
• MyVariant Identifiers: chr9:g.377032C>G (hg19) ; chr9:g.377032C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.377032C>G , CM000671.2:g.377032C>G	GRCh38
NC_000009.11:g.377032C>G , CM000671.1:g.377032C>G	GRCh37
NC_000009.10:g.367032C>G	NCBI36
NG_017007.1:g.167168C>G , LRG_196:g.167168C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.2057C>G	ENSP00000371766.2:p.Thr686Ser
ENST00000382331.6:n.758C>G
ENST00000483757.6:c.*948C>G	ENSP00000417691.2:n.*948C>G
ENST00000682260.1:n.2157C>G
ENST00000685949.1:n.1049C>G
ENST00000432829.7:c.2261C>G MANE Select	ENSP00000394888.3:p.Thr754Ser
ENST00000382329.1:c.662C>G	ENSP00000371766.1:p.Thr221Ser
ENST00000382331.5:c.167C>G	ENSP00000371768.1:p.Thr56Ser
ENST00000432829.6:c.2261C>G	ENSP00000394888.3:p.Thr754Ser
ENST00000453981.5:c.2057C>G	ENSP00000408464.2:p.Thr686Ser
ENST00000469391.5:c.2057C>G	ENSP00000419438.1:p.Thr686Ser
ENST00000483757.5:c.*1736C>G	ENSP00000417691.1:n.*1736C>G
ENST00000495184.5:n.4216C>G
NM_001190458.1:c.2057C>G	NP_001177387.1:p.Thr686Ser
NM_001193536.1:c.2057C>G	NP_001180465.1:p.Thr686Ser
NM_203447.3:c.2261C>G , LRG_196t1:c.2261C>G	NP_982272.2:p.Thr754Ser
XM_011518045.1:c.2057C>G	XP_011516347.1:p.Thr686Ser
XM_011518046.1:c.2123C>G	XP_011516348.1:p.Thr708Ser
XM_011518047.1:c.2057C>G	XP_011516349.1:p.Thr686Ser
XM_011518048.1:c.2057C>G	XP_011516350.1:p.Thr686Ser
XM_011518049.1:c.497C>G	XP_011516351.1:p.Thr166Ser
XM_011518045.3:c.2057C>G	XP_011516347.1:p.Thr686Ser
XM_011518046.2:c.2123C>G	XP_011516348.1:p.Thr708Ser
XM_011518047.3:c.2057C>G	XP_011516349.1:p.Thr686Ser
XM_011518048.2:c.2057C>G	XP_011516350.1:p.Thr686Ser
XM_011518049.2:c.497C>G	XP_011516351.1:p.Thr166Ser
XM_017015173.1:c.2057C>G	XP_016870662.1:p.Thr686Ser
XM_017015174.1:c.2123C>G	XP_016870663.1:p.Thr708Ser
NM_001190458.2:c.2057C>G	NP_001177387.1:p.Thr686Ser
NM_001193536.2:c.2057C>G	NP_001180465.1:p.Thr686Ser
NM_203447.4:c.2261C>G MANE Select	NP_982272.2:p.Thr754Ser