Canonical Allele Identifier: CA372752226

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.271642A>C (hg19) ; chr9:g.271642A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.271642A>C , CM000671.2:g.271642A>C	GRCh38
NC_000009.11:g.271642A>C , CM000671.1:g.271642A>C	GRCh37
NC_000009.10:g.261642A>C	NCBI36
NG_017007.1:g.61778A>C , LRG_196:g.61778A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.-136A>C	ENSP00000371766.2:n.-136A>C
ENST00000682121.1:n.166-14819A>C
ENST00000684166.1:n.178A>C
ENST00000684384.1:n.178A>C
ENST00000432829.7:c.69A>C MANE Select	ENSP00000394888.3:p.Glu23Asp
ENST00000432829.6:c.69A>C	ENSP00000394888.3:p.Glu23Asp
ENST00000454469.6:n.178A>C
ENST00000469197.5:c.69A>C	ENSP00000418587.1:p.Glu23Asp
ENST00000479404.5:c.-136A>C	ENSP00000417082.1:n.-136A>C
ENST00000524396.5:c.*32A>C	ENSP00000436628.1:n.*32A>C
NM_203447.3:c.69A>C , LRG_196t1:c.69A>C	NP_982272.2:p.Glu23Asp
XM_011518045.1:c.-136A>C	XP_011516347.1:n.-136A>C
XM_011518047.1:c.-136A>C	XP_011516349.1:n.-136A>C
XR_929404.1:n.88+1263T>G
XR_929406.1:n.1333+2642T>G
XM_011518045.3:c.-136A>C	XP_011516347.1:n.-136A>C
XM_011518047.3:c.-136A>C	XP_011516349.1:n.-136A>C
XM_017015173.1:c.-136A>C	XP_016870662.1:n.-136A>C
NM_203447.4:c.69A>C MANE Select	NP_982272.2:p.Glu23Asp