Canonical Allele Identifier: CA463677882

Gene: DOCK8

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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