Canonical Allele Identifier: CA372768164

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.441394G>T (hg19) ; chr9:g.441394G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.441394G>T , CM000671.2:g.441394G>T	GRCh38
NC_000009.11:g.441394G>T , CM000671.1:g.441394G>T	GRCh37
NC_000009.10:g.431394G>T	NCBI36
NG_017007.1:g.231530G>T , LRG_196:g.231530G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5032G>T	ENSP00000371766.2:p.Ala1678Ser
ENST00000683406.1:n.1807G>T
ENST00000684637.1:n.1013G>T
ENST00000685949.1:n.4120G>T
ENST00000432829.7:c.5332G>T MANE Select	ENSP00000394888.3:p.Ala1778Ser
ENST00000382329.1:c.3733G>T	ENSP00000371766.1:p.Ala1245Ser
ENST00000432829.6:c.5332G>T	ENSP00000394888.3:p.Ala1778Ser
ENST00000453981.5:c.5128G>T	ENSP00000408464.2:p.Ala1710Ser
ENST00000469391.5:c.5032G>T	ENSP00000419438.1:p.Ala1678Ser
ENST00000495184.5:n.7287G>T
NM_001190458.1:c.5032G>T	NP_001177387.1:p.Ala1678Ser
NM_001193536.1:c.5128G>T	NP_001180465.1:p.Ala1710Ser
NM_203447.3:c.5332G>T , LRG_196t1:c.5332G>T	NP_982272.2:p.Ala1778Ser
XM_011518045.1:c.5032G>T	XP_011516347.1:p.Ala1678Ser
XM_011518046.1:c.5194G>T	XP_011516348.1:p.Ala1732Ser
XM_011518047.1:c.5128G>T	XP_011516349.1:p.Ala1710Ser
XM_011518048.1:c.5128G>T	XP_011516350.1:p.Ala1710Ser
XM_011518049.1:c.3568G>T	XP_011516351.1:p.Ala1190Ser
XM_011518045.3:c.5032G>T	XP_011516347.1:p.Ala1678Ser
XM_011518046.2:c.5194G>T	XP_011516348.1:p.Ala1732Ser
XM_011518047.3:c.5128G>T	XP_011516349.1:p.Ala1710Ser
XM_011518048.2:c.5128G>T	XP_011516350.1:p.Ala1710Ser
XM_011518049.2:c.3568G>T	XP_011516351.1:p.Ala1190Ser
XM_017015173.1:c.5128G>T	XP_016870662.1:p.Ala1710Ser
XM_017015174.1:c.5194G>T	XP_016870663.1:p.Ala1732Ser
NM_001190458.2:c.5032G>T	NP_001177387.1:p.Ala1678Ser
NM_001193536.2:c.5128G>T	NP_001180465.1:p.Ala1710Ser
NM_203447.4:c.5332G>T MANE Select	NP_982272.2:p.Ala1778Ser