Canonical Allele Identifier: CA4959339

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.439370C>T , CM000671.2:g.439370C>T	GRCh38
NC_000009.11:g.439370C>T , CM000671.1:g.439370C>T	GRCh37
NC_000009.10:g.429370C>T	NCBI36
NG_017007.1:g.229506C>T , LRG_196:g.229506C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_203447.4:c.5205C>T MANE Select	NP_982272.2:p.Ala1735=
ENST00000432829.7:c.5205C>T MANE Select	ENSP00000394888.3:p.Ala1735=
NM_001190458.1:c.4905C>T	NP_001177387.1:p.Ala1635=
NM_001190458.2:c.4905C>T	NP_001177387.1:p.Ala1635=
NM_001193536.1:c.5001C>T	NP_001180465.1:p.Ala1667=
NM_001193536.2:c.5001C>T	NP_001180465.1:p.Ala1667=
NM_203447.3:c.5205C>T , LRG_196t1:c.5205C>T	NP_982272.2:p.Ala1735=
ENST00000382329.1:c.3606C>T	ENSP00000371766.1:p.Ala1202=
ENST00000382329.2:c.4905C>T	ENSP00000371766.2:p.Ala1635=
ENST00000432829.6:c.5205C>T	ENSP00000394888.3:p.Ala1735=
ENST00000453981.5:c.5001C>T	ENSP00000408464.2:p.Ala1667=
ENST00000469391.5:c.4905C>T	ENSP00000419438.1:p.Ala1635=
ENST00000495184.5:n.7160C>T
ENST00000683406.1:n.1680C>T
ENST00000685949.1:n.3993C>T
XM_011518045.1:c.4905C>T	XP_011516347.1:p.Ala1635=
XM_011518045.3:c.4905C>T	XP_011516347.1:p.Ala1635=
XM_011518046.1:c.5067C>T	XP_011516348.1:p.Ala1689=
XM_011518046.2:c.5067C>T	XP_011516348.1:p.Ala1689=
XM_011518047.1:c.5001C>T	XP_011516349.1:p.Ala1667=
XM_011518047.3:c.5001C>T	XP_011516349.1:p.Ala1667=
XM_011518048.1:c.5001C>T	XP_011516350.1:p.Ala1667=
XM_011518048.2:c.5001C>T	XP_011516350.1:p.Ala1667=
XM_011518049.1:c.3441C>T	XP_011516351.1:p.Ala1147=
XM_011518049.2:c.3441C>T	XP_011516351.1:p.Ala1147=
XM_017015173.1:c.5001C>T	XP_016870662.1:p.Ala1667=
XM_017015174.1:c.5067C>T	XP_016870663.1:p.Ala1689=