Canonical Allele Identifier: CA1734883700

Gene: DOCK4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.112156322A= , CM000669.2:g.112156322A=	GRCh38
NC_000007.13:g.111796377A= , CM000669.1:g.111796377A=	GRCh37
NC_000007.12:g.111583613A=	NCBI36
NG_028060.1:g.55086T=
NG_028060.2:g.55090T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428084.6:c.37+49780T= MANE Select	ENSP00000410746.1:n.37+49780T=
ENST00000437633.6:c.37+49780T=	ENSP00000404179.1:n.37+49780T=
ENST00000661654.1:n.306+49780T=
ENST00000428084.5:c.37+49780T=	ENSP00000410746.1:n.37+49780T=
ENST00000437633.5:c.37+49780T=	ENSP00000404179.1:n.37+49780T=
ENST00000476846.5:n.293+49780T=
NM_014705.3:c.37+49780T=	NP_055520.3:n.37+49780T=
XM_006716188.1:c.37+49780T=	XP_006716251.1:n.37+49780T=
XM_006716189.1:c.37+49780T=	XP_006716252.1:n.37+49780T=
XM_011516716.1:c.37+49780T=	XP_011515018.1:n.37+49780T=
XM_011516717.1:c.37+49780T=	XP_011515019.1:n.37+49780T=
NM_001363540.1:c.37+49780T=	NP_001350469.1:n.37+49780T=
XM_006716189.2:c.37+49780T=	XP_006716252.1:n.37+49780T=
XM_017012819.1:c.130+49051T=	XP_016868308.1:n.130+49051T=
XM_017012820.1:c.130+49051T=	XP_016868309.1:n.130+49051T=
XM_017012821.1:c.130+49051T=	XP_016868310.1:n.130+49051T=
XM_017012823.1:c.130+49051T=	XP_016868312.1:n.130+49051T=
XM_017012824.1:c.130+49051T=	XP_016868313.1:n.130+49051T=
XM_017012825.1:c.130+49051T=	XP_016868314.1:n.130+49051T=
XM_024447006.1:c.-192+49176T=	XP_024302774.1:n.-192+49176T=
NM_014705.4:c.37+49780T=	NP_055520.3:n.37+49780T=
NM_001363540.2:c.37+49780T= MANE Select	NP_001350469.1:n.37+49780T=