Canonical Allele Identifier: CA463677885

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.271636A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.271636A>G , CM000671.2:g.271636A>G	GRCh38
NC_000009.11:g.271636A>G , CM000671.1:g.271636A>G	GRCh37
NC_000009.10:g.261636A>G	NCBI36
NG_017007.1:g.61772A>G , LRG_196:g.61772A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.-142A>G	ENSP00000371766.2:n.-142A>G
ENST00000682121.1:n.166-14825A>G
ENST00000684166.1:n.172A>G
ENST00000684384.1:n.172A>G
ENST00000432829.7:c.63A>G MANE Select	ENSP00000394888.3:p.Ser21=
ENST00000432829.6:c.63A>G	ENSP00000394888.3:p.Ser21=
ENST00000454469.6:n.172A>G
ENST00000469197.5:c.63A>G	ENSP00000418587.1:p.Ser21=
ENST00000479404.5:c.-142A>G	ENSP00000417082.1:n.-142A>G
ENST00000524396.5:c.*26A>G	ENSP00000436628.1:n.*26A>G
NM_203447.3:c.63A>G , LRG_196t1:c.63A>G	NP_982272.2:p.Ser21=
XM_011518045.1:c.-142A>G	XP_011516347.1:n.-142A>G
XM_011518047.1:c.-142A>G	XP_011516349.1:n.-142A>G
XR_929404.1:n.88+1269T>C
XR_929406.1:n.1333+2648T>C
XM_011518045.3:c.-142A>G	XP_011516347.1:n.-142A>G
XM_011518047.3:c.-142A>G	XP_011516349.1:n.-142A>G
XM_017015173.1:c.-142A>G	XP_016870662.1:n.-142A>G
NM_203447.4:c.63A>G MANE Select	NP_982272.2:p.Ser21=