Canonical Allele Identifier: CA1734818349

Gene: DOCK4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.112002502_112002505delinsCTTA , CM000669.2:g.112002502_112002505delinsCTTA	GRCh38
NC_000007.13:g.111642557_111642560delinsCTTA , CM000669.1:g.111642557_111642560delinsCTTA	GRCh37
NC_000007.12:g.111429793_111429796delinsCTTA	NCBI36
NG_028060.1:g.208903_208906delinsTAAG
NG_028060.2:g.208907_208910delinsTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428084.6:c.121+1543_121+1546delinsTAAG MANE Select	ENSP00000410746.1:n.121+1543_121+1546delinsTAAG
ENST00000437633.6:c.121+1543_121+1546delinsTAAG	ENSP00000404179.1:n.121+1543_121+1546delinsTAAG
ENST00000494651.7:c.85+1543_85+1546delinsTAAG	ENSP00000440944.3:n.85+1543_85+1546delinsTAAG
ENST00000661654.1:n.390+1543_390+1546delinsTAAG
ENST00000428084.5:c.121+1543_121+1546delinsTAAG	ENSP00000410746.1:n.121+1543_121+1546delinsTAAG
ENST00000437633.5:c.121+1543_121+1546delinsTAAG	ENSP00000404179.1:n.121+1543_121+1546delinsTAAG
ENST00000445943.5:c.84+1543_84+1546delinsTAAG
ENST00000468571.1:n.85+1543_85+1546delinsTAAG
ENST00000476846.5:n.377+1543_377+1546delinsTAAG
ENST00000494651.6:c.85+1543_85+1546delinsTAAG	ENSP00000440944.2:n.85+1543_85+1546delinsTAAG
NM_014705.3:c.121+1543_121+1546delinsTAAG	NP_055520.3:n.121+1543_121+1546delinsTAAG
XM_006716188.1:c.121+1543_121+1546delinsTAAG	XP_006716251.1:n.121+1543_121+1546delinsTAAG
XM_006716189.1:c.121+1543_121+1546delinsTAAG	XP_006716252.1:n.121+1543_121+1546delinsTAAG
XM_011516716.1:c.121+1543_121+1546delinsTAAG	XP_011515018.1:n.121+1543_121+1546delinsTAAG
XM_011516717.1:c.121+1543_121+1546delinsTAAG	XP_011515019.1:n.121+1543_121+1546delinsTAAG
NM_001363540.1:c.121+1543_121+1546delinsTAAG	NP_001350469.1:n.121+1543_121+1546delinsTAAG
XM_006716189.2:c.121+1543_121+1546delinsTAAG	XP_006716252.1:n.121+1543_121+1546delinsTAAG
XM_017012819.1:c.214+1543_214+1546delinsTAAG	XP_016868308.1:n.214+1543_214+1546delinsTAAG
XM_017012820.1:c.214+1543_214+1546delinsTAAG	XP_016868309.1:n.214+1543_214+1546delinsTAAG
XM_017012821.1:c.214+1543_214+1546delinsTAAG	XP_016868310.1:n.214+1543_214+1546delinsTAAG
XM_017012822.1:c.154+1543_154+1546delinsTAAG	XP_016868311.1:n.154+1543_154+1546delinsTAAG
XM_017012823.1:c.214+1543_214+1546delinsTAAG	XP_016868312.1:n.214+1543_214+1546delinsTAAG
XM_017012824.1:c.214+1543_214+1546delinsTAAG	XP_016868313.1:n.214+1543_214+1546delinsTAAG
XM_017012825.1:c.214+1543_214+1546delinsTAAG	XP_016868314.1:n.214+1543_214+1546delinsTAAG
XM_024447006.1:c.-108+1543_-108+1546delinsTAAG	XP_024302774.1:n.-108+1543_-108+1546delinsTAAG
NM_014705.4:c.121+1543_121+1546delinsTAAG	NP_055520.3:n.121+1543_121+1546delinsTAAG
NM_001363540.2:c.121+1543_121+1546delinsTAAG MANE Select	NP_001350469.1:n.121+1543_121+1546delinsTAAG