Canonical Allele Identifier: CA1734818330

Gene: DOCK4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.112002463_112002464delinsAG , CM000669.2:g.112002463_112002464delinsAG	GRCh38
NC_000007.13:g.111642518_111642519delinsAG , CM000669.1:g.111642518_111642519delinsAG	GRCh37
NC_000007.12:g.111429754_111429755delinsAG	NCBI36
NG_028060.1:g.208944_208945delinsCT
NG_028060.2:g.208948_208949delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428084.6:c.121+1584_121+1585delinsCT MANE Select	ENSP00000410746.1:n.121+1584_121+1585delinsCT
ENST00000437633.6:c.121+1584_121+1585delinsCT	ENSP00000404179.1:n.121+1584_121+1585delinsCT
ENST00000494651.7:c.85+1584_85+1585delinsCT	ENSP00000440944.3:n.85+1584_85+1585delinsCT
ENST00000661654.1:n.390+1584_390+1585delinsCT
ENST00000428084.5:c.121+1584_121+1585delinsCT	ENSP00000410746.1:n.121+1584_121+1585delinsCT
ENST00000437633.5:c.121+1584_121+1585delinsCT	ENSP00000404179.1:n.121+1584_121+1585delinsCT
ENST00000445943.5:c.84+1584_84+1585delinsCT
ENST00000468571.1:n.85+1584_85+1585delinsCT
ENST00000476846.5:n.377+1584_377+1585delinsCT
ENST00000494651.6:c.85+1584_85+1585delinsCT	ENSP00000440944.2:n.85+1584_85+1585delinsCT
NM_014705.3:c.121+1584_121+1585delinsCT	NP_055520.3:n.121+1584_121+1585delinsCT
XM_006716188.1:c.121+1584_121+1585delinsCT	XP_006716251.1:n.121+1584_121+1585delinsCT
XM_006716189.1:c.121+1584_121+1585delinsCT	XP_006716252.1:n.121+1584_121+1585delinsCT
XM_011516716.1:c.121+1584_121+1585delinsCT	XP_011515018.1:n.121+1584_121+1585delinsCT
XM_011516717.1:c.121+1584_121+1585delinsCT	XP_011515019.1:n.121+1584_121+1585delinsCT
NM_001363540.1:c.121+1584_121+1585delinsCT	NP_001350469.1:n.121+1584_121+1585delinsCT
XM_006716189.2:c.121+1584_121+1585delinsCT	XP_006716252.1:n.121+1584_121+1585delinsCT
XM_017012819.1:c.214+1584_214+1585delinsCT	XP_016868308.1:n.214+1584_214+1585delinsCT
XM_017012820.1:c.214+1584_214+1585delinsCT	XP_016868309.1:n.214+1584_214+1585delinsCT
XM_017012821.1:c.214+1584_214+1585delinsCT	XP_016868310.1:n.214+1584_214+1585delinsCT
XM_017012822.1:c.154+1584_154+1585delinsCT	XP_016868311.1:n.154+1584_154+1585delinsCT
XM_017012823.1:c.214+1584_214+1585delinsCT	XP_016868312.1:n.214+1584_214+1585delinsCT
XM_017012824.1:c.214+1584_214+1585delinsCT	XP_016868313.1:n.214+1584_214+1585delinsCT
XM_017012825.1:c.214+1584_214+1585delinsCT	XP_016868314.1:n.214+1584_214+1585delinsCT
XM_024447006.1:c.-108+1584_-108+1585delinsCT	XP_024302774.1:n.-108+1584_-108+1585delinsCT
NM_014705.4:c.121+1584_121+1585delinsCT	NP_055520.3:n.121+1584_121+1585delinsCT
NM_001363540.2:c.121+1584_121+1585delinsCT MANE Select	NP_001350469.1:n.121+1584_121+1585delinsCT