Canonical Allele Identifier: CA463691091

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.414902T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414902T>G , CM000671.2:g.414902T>G	GRCh38
NC_000009.11:g.414902T>G , CM000671.1:g.414902T>G	GRCh37
NC_000009.10:g.404902T>G	NCBI36
NG_017007.1:g.205038T>G , LRG_196:g.205038T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3351T>G	ENSP00000371766.2:p.Pro1117=
ENST00000683406.1:n.172T>G
ENST00000685949.1:n.2439T>G
ENST00000432829.7:c.3651T>G MANE Select	ENSP00000394888.3:p.Pro1217=
ENST00000382329.1:c.2052T>G	ENSP00000371766.1:p.Pro684=
ENST00000432829.6:c.3651T>G	ENSP00000394888.3:p.Pro1217=
ENST00000453981.5:c.3447T>G	ENSP00000408464.2:p.Pro1149=
ENST00000469391.5:c.3351T>G	ENSP00000419438.1:p.Pro1117=
ENST00000495184.5:n.5606T>G
NM_001190458.1:c.3351T>G	NP_001177387.1:p.Pro1117=
NM_001193536.1:c.3447T>G	NP_001180465.1:p.Pro1149=
NM_203447.3:c.3651T>G , LRG_196t1:c.3651T>G	NP_982272.2:p.Pro1217=
XM_011518045.1:c.3351T>G	XP_011516347.1:p.Pro1117=
XM_011518046.1:c.3513T>G	XP_011516348.1:p.Pro1171=
XM_011518047.1:c.3447T>G	XP_011516349.1:p.Pro1149=
XM_011518048.1:c.3447T>G	XP_011516350.1:p.Pro1149=
XM_011518049.1:c.1887T>G	XP_011516351.1:p.Pro629=
XM_011518045.3:c.3351T>G	XP_011516347.1:p.Pro1117=
XM_011518046.2:c.3513T>G	XP_011516348.1:p.Pro1171=
XM_011518047.3:c.3447T>G	XP_011516349.1:p.Pro1149=
XM_011518048.2:c.3447T>G	XP_011516350.1:p.Pro1149=
XM_011518049.2:c.1887T>G	XP_011516351.1:p.Pro629=
XM_017015173.1:c.3447T>G	XP_016870662.1:p.Pro1149=
XM_017015174.1:c.3513T>G	XP_016870663.1:p.Pro1171=
NM_001190458.2:c.3351T>G	NP_001177387.1:p.Pro1117=
NM_001193536.2:c.3447T>G	NP_001180465.1:p.Pro1149=
NM_203447.4:c.3651T>G MANE Select	NP_982272.2:p.Pro1217=