Canonical Allele Identifier: CA4959164

Gene: DOCK8

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.432163C>T , CM000671.2:g.432163C>T	GRCh38
NC_000009.11:g.432163C>T , CM000671.1:g.432163C>T	GRCh37
NC_000009.10:g.422163C>T	NCBI36
NG_017007.1:g.222299C>T , LRG_196:g.222299C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.4327-3C>T	ENSP00000371766.2:n.4327-3C>T
ENST00000683406.1:n.1148-3C>T
ENST00000685949.1:n.3415-3C>T
ENST00000432829.7:c.4627-3C>T MANE Select	ENSP00000394888.3:n.4627-3C>T
ENST00000382329.1:c.3028-3C>T	ENSP00000371766.1:n.3028-3C>T
ENST00000432829.6:c.4627-3C>T	ENSP00000394888.3:n.4627-3C>T
ENST00000453981.5:c.4423-3C>T	ENSP00000408464.2:n.4423-3C>T
ENST00000469391.5:c.4327-3C>T	ENSP00000419438.1:n.4327-3C>T
ENST00000495184.5:n.6582-3C>T
NM_001190458.1:c.4327-3C>T	NP_001177387.1:n.4327-3C>T
NM_001193536.1:c.4423-3C>T	NP_001180465.1:n.4423-3C>T
NM_203447.3:c.4627-3C>T , LRG_196t1:c.4627-3C>T	NP_982272.2:n.4627-3C>T
XM_011518045.1:c.4327-3C>T	XP_011516347.1:n.4327-3C>T
XM_011518046.1:c.4489-3C>T	XP_011516348.1:n.4489-3C>T
XM_011518047.1:c.4423-3C>T	XP_011516349.1:n.4423-3C>T
XM_011518048.1:c.4423-3C>T	XP_011516350.1:n.4423-3C>T
XM_011518049.1:c.2863-3C>T	XP_011516351.1:n.2863-3C>T
XM_011518045.3:c.4327-3C>T	XP_011516347.1:n.4327-3C>T
XM_011518046.2:c.4489-3C>T	XP_011516348.1:n.4489-3C>T
XM_011518047.3:c.4423-3C>T	XP_011516349.1:n.4423-3C>T
XM_011518048.2:c.4423-3C>T	XP_011516350.1:n.4423-3C>T
XM_011518049.2:c.2863-3C>T	XP_011516351.1:n.2863-3C>T
XM_017015173.1:c.4423-3C>T	XP_016870662.1:n.4423-3C>T
XM_017015174.1:c.4489-3C>T	XP_016870663.1:n.4489-3C>T
NM_001190458.2:c.4327-3C>T	NP_001177387.1:n.4327-3C>T
NM_001193536.2:c.4423-3C>T	NP_001180465.1:n.4423-3C>T
NM_203447.4:c.4627-3C>T MANE Select	NP_982272.2:n.4627-3C>T