Canonical Allele Identifier: CA463701296
Gene: DOCK8 HGNC NCBI

Linked Data

dbSNP Id: rs1412147554
MyVariant Identifiers: chr9:g.452103G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.452103G>A , CM000671.2:g.452103G>A GRCh38
NC_000009.11:g.452103G>A , CM000671.1:g.452103G>A GRCh37
NC_000009.10:g.442103G>A NCBI36
NG_017007.1:g.242239G>A , LRG_196:g.242239G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.5754G>A ENSP00000371766.2:p.Lys1918=
ENST00000683406.1:n.2529G>A
ENST00000684637.1:n.1735G>A
ENST00000685949.1:n.4842G>A
ENST00000432829.7:c.6054G>A MANE Select ENSP00000394888.3:p.Lys2018=
ENST00000382329.1:c.4455G>A ENSP00000371766.1:p.Lys1485=
ENST00000432829.6:c.6054G>A ENSP00000394888.3:p.Lys2018=
ENST00000453981.5:c.5850G>A ENSP00000408464.2:p.Lys1950=
ENST00000469391.5:c.5754G>A ENSP00000419438.1:p.Lys1918=
ENST00000495184.5:n.8009G>A
NM_001190458.1:c.5754G>A NP_001177387.1:p.Lys1918=
NM_001193536.1:c.5850G>A NP_001180465.1:p.Lys1950=
NM_203447.3:c.6054G>A , LRG_196t1:c.6054G>A NP_982272.2:p.Lys2018=
XM_011518045.1:c.5754G>A XP_011516347.1:p.Lys1918=
XM_011518046.1:c.5916G>A XP_011516348.1:p.Lys1972=
XM_011518047.1:c.5850G>A XP_011516349.1:p.Lys1950=
XM_011518048.1:c.5850G>A XP_011516350.1:p.Lys1950=
XM_011518049.1:c.4290G>A XP_011516351.1:p.Lys1430=
XM_011518045.3:c.5754G>A XP_011516347.1:p.Lys1918=
XM_011518046.2:c.5916G>A XP_011516348.1:p.Lys1972=
XM_011518047.3:c.5850G>A XP_011516349.1:p.Lys1950=
XM_011518048.2:c.5850G>A XP_011516350.1:p.Lys1950=
XM_011518049.2:c.4290G>A XP_011516351.1:p.Lys1430=
XM_017015173.1:c.5850G>A XP_016870662.1:p.Lys1950=
XM_017015174.1:c.5916G>A XP_016870663.1:p.Lys1972=
NM_001190458.2:c.5754G>A NP_001177387.1:p.Lys1918=
NM_001193536.2:c.5850G>A NP_001180465.1:p.Lys1950=
NM_203447.4:c.6054G>A MANE Select NP_982272.2:p.Lys2018=