Canonical Allele Identifier: CA372760842

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.414894T>G (hg19) ; chr9:g.414894T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414894T>G , CM000671.2:g.414894T>G	GRCh38
NC_000009.11:g.414894T>G , CM000671.1:g.414894T>G	GRCh37
NC_000009.10:g.404894T>G	NCBI36
NG_017007.1:g.205030T>G , LRG_196:g.205030T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3343T>G	ENSP00000371766.2:p.Tyr1115Asp
ENST00000683406.1:n.164T>G
ENST00000685949.1:n.2431T>G
ENST00000432829.7:c.3643T>G MANE Select	ENSP00000394888.3:p.Tyr1215Asp
ENST00000382329.1:c.2044T>G	ENSP00000371766.1:p.Tyr682Asp
ENST00000432829.6:c.3643T>G	ENSP00000394888.3:p.Tyr1215Asp
ENST00000453981.5:c.3439T>G	ENSP00000408464.2:p.Tyr1147Asp
ENST00000469391.5:c.3343T>G	ENSP00000419438.1:p.Tyr1115Asp
ENST00000495184.5:n.5598T>G
NM_001190458.1:c.3343T>G	NP_001177387.1:p.Tyr1115Asp
NM_001193536.1:c.3439T>G	NP_001180465.1:p.Tyr1147Asp
NM_203447.3:c.3643T>G , LRG_196t1:c.3643T>G	NP_982272.2:p.Tyr1215Asp
XM_011518045.1:c.3343T>G	XP_011516347.1:p.Tyr1115Asp
XM_011518046.1:c.3505T>G	XP_011516348.1:p.Tyr1169Asp
XM_011518047.1:c.3439T>G	XP_011516349.1:p.Tyr1147Asp
XM_011518048.1:c.3439T>G	XP_011516350.1:p.Tyr1147Asp
XM_011518049.1:c.1879T>G	XP_011516351.1:p.Tyr627Asp
XM_011518045.3:c.3343T>G	XP_011516347.1:p.Tyr1115Asp
XM_011518046.2:c.3505T>G	XP_011516348.1:p.Tyr1169Asp
XM_011518047.3:c.3439T>G	XP_011516349.1:p.Tyr1147Asp
XM_011518048.2:c.3439T>G	XP_011516350.1:p.Tyr1147Asp
XM_011518049.2:c.1879T>G	XP_011516351.1:p.Tyr627Asp
XM_017015173.1:c.3439T>G	XP_016870662.1:p.Tyr1147Asp
XM_017015174.1:c.3505T>G	XP_016870663.1:p.Tyr1169Asp
NM_001190458.2:c.3343T>G	NP_001177387.1:p.Tyr1115Asp
NM_001193536.2:c.3439T>G	NP_001180465.1:p.Tyr1147Asp
NM_203447.4:c.3643T>G MANE Select	NP_982272.2:p.Tyr1215Asp