Canonical Allele Identifier: CA463691080

Gene: DOCK8

Linked Data

• gnomAD v4: 9-414890-C-G
• MyVariant Identifiers: chr9:g.414890C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414890C>G , CM000671.2:g.414890C>G	GRCh38
NC_000009.11:g.414890C>G , CM000671.1:g.414890C>G	GRCh37
NC_000009.10:g.404890C>G	NCBI36
NG_017007.1:g.205026C>G , LRG_196:g.205026C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3339C>G	ENSP00000371766.2:p.Ala1113=
ENST00000683406.1:n.160C>G
ENST00000685949.1:n.2427C>G
ENST00000432829.7:c.3639C>G MANE Select	ENSP00000394888.3:p.Ala1213=
ENST00000382329.1:c.2040C>G	ENSP00000371766.1:p.Ala680=
ENST00000432829.6:c.3639C>G	ENSP00000394888.3:p.Ala1213=
ENST00000453981.5:c.3435C>G	ENSP00000408464.2:p.Ala1145=
ENST00000469391.5:c.3339C>G	ENSP00000419438.1:p.Ala1113=
ENST00000495184.5:n.5594C>G
NM_001190458.1:c.3339C>G	NP_001177387.1:p.Ala1113=
NM_001193536.1:c.3435C>G	NP_001180465.1:p.Ala1145=
NM_203447.3:c.3639C>G , LRG_196t1:c.3639C>G	NP_982272.2:p.Ala1213=
XM_011518045.1:c.3339C>G	XP_011516347.1:p.Ala1113=
XM_011518046.1:c.3501C>G	XP_011516348.1:p.Ala1167=
XM_011518047.1:c.3435C>G	XP_011516349.1:p.Ala1145=
XM_011518048.1:c.3435C>G	XP_011516350.1:p.Ala1145=
XM_011518049.1:c.1875C>G	XP_011516351.1:p.Ala625=
XM_011518045.3:c.3339C>G	XP_011516347.1:p.Ala1113=
XM_011518046.2:c.3501C>G	XP_011516348.1:p.Ala1167=
XM_011518047.3:c.3435C>G	XP_011516349.1:p.Ala1145=
XM_011518048.2:c.3435C>G	XP_011516350.1:p.Ala1145=
XM_011518049.2:c.1875C>G	XP_011516351.1:p.Ala625=
XM_017015173.1:c.3435C>G	XP_016870662.1:p.Ala1145=
XM_017015174.1:c.3501C>G	XP_016870663.1:p.Ala1167=
NM_001190458.2:c.3339C>G	NP_001177387.1:p.Ala1113=
NM_001193536.2:c.3435C>G	NP_001180465.1:p.Ala1145=
NM_203447.4:c.3639C>G MANE Select	NP_982272.2:p.Ala1213=