Canonical Allele Identifier: CA463701254

Gene: DOCK8

Linked Data

• MyVariant Identifiers: chr9:g.452037T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.452037T>C , CM000671.2:g.452037T>C	GRCh38
NC_000009.11:g.452037T>C , CM000671.1:g.452037T>C	GRCh37
NC_000009.10:g.442037T>C	NCBI36
NG_017007.1:g.242173T>C , LRG_196:g.242173T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5688T>C	ENSP00000371766.2:p.Phe1896=
ENST00000683406.1:n.2463T>C
ENST00000684637.1:n.1669T>C
ENST00000685949.1:n.4776T>C
ENST00000432829.7:c.5988T>C MANE Select	ENSP00000394888.3:p.Phe1996=
ENST00000382329.1:c.4389T>C	ENSP00000371766.1:p.Phe1463=
ENST00000432829.6:c.5988T>C	ENSP00000394888.3:p.Phe1996=
ENST00000453981.5:c.5784T>C	ENSP00000408464.2:p.Phe1928=
ENST00000469391.5:c.5688T>C	ENSP00000419438.1:p.Phe1896=
ENST00000495184.5:n.7943T>C
NM_001190458.1:c.5688T>C	NP_001177387.1:p.Phe1896=
NM_001193536.1:c.5784T>C	NP_001180465.1:p.Phe1928=
NM_203447.3:c.5988T>C , LRG_196t1:c.5988T>C	NP_982272.2:p.Phe1996=
XM_011518045.1:c.5688T>C	XP_011516347.1:p.Phe1896=
XM_011518046.1:c.5850T>C	XP_011516348.1:p.Phe1950=
XM_011518047.1:c.5784T>C	XP_011516349.1:p.Phe1928=
XM_011518048.1:c.5784T>C	XP_011516350.1:p.Phe1928=
XM_011518049.1:c.4224T>C	XP_011516351.1:p.Phe1408=
XM_011518045.3:c.5688T>C	XP_011516347.1:p.Phe1896=
XM_011518046.2:c.5850T>C	XP_011516348.1:p.Phe1950=
XM_011518047.3:c.5784T>C	XP_011516349.1:p.Phe1928=
XM_011518048.2:c.5784T>C	XP_011516350.1:p.Phe1928=
XM_011518049.2:c.4224T>C	XP_011516351.1:p.Phe1408=
XM_017015173.1:c.5784T>C	XP_016870662.1:p.Phe1928=
XM_017015174.1:c.5850T>C	XP_016870663.1:p.Phe1950=
NM_001190458.2:c.5688T>C	NP_001177387.1:p.Phe1896=
NM_001193536.2:c.5784T>C	NP_001180465.1:p.Phe1928=
NM_203447.4:c.5988T>C MANE Select	NP_982272.2:p.Phe1996=