Canonical Allele Identifier: CA4956878

Gene: DOCK8 DOCK8-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.214908T>C , CM000671.2:g.214908T>C	GRCh38
NC_000009.11:g.214908T>C , CM000671.1:g.214908T>C	GRCh37
NC_000009.10:g.204908T>C	NCBI36
NG_017007.1:g.5044T>C , LRG_196:g.5044T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_203447.4:c.-69T>C (DOCK8) MANE Select	NP_982272.2:n.-69T>C
ENST00000432829.7:c.-69T>C (DOCK8) MANE Select	ENSP00000394888.3:n.-69T>C
NM_152569.2:c.489A>G (DOCK8-AS1)	NP_689782.2:p.Arg163=
NM_203447.3:c.-69T>C , LRG_196t1:c.-69T>C (DOCK8)	NP_982272.2:n.-69T>C
NR_160804.1:n.843A>G (DOCK8-AS1)
ENST00000382387.3:c.489A>G (DOCK8-AS1)	ENSP00000371824.2:p.Arg163=
ENST00000432829.6:c.-69T>C (DOCK8)	ENSP00000394888.3:n.-69T>C
ENST00000454469.6:n.41T>C (DOCK8)
ENST00000469197.5:c.-69T>C (DOCK8)	ENSP00000418587.1:n.-69T>C
ENST00000524396.5:c.-69T>C (DOCK8)	ENSP00000436628.1:n.-69T>C
ENST00000682121.1:n.44T>C (DOCK8)
ENST00000684166.1:n.41T>C (DOCK8)
ENST00000684384.1:n.41T>C (DOCK8)
XM_011518045.3:c.-152+3592T>C (DOCK8)	XP_011516347.1:n.-152+3592T>C
XM_017015173.1:c.-152+3592T>C (DOCK8)	XP_016870662.1:n.-152+3592T>C