Canonical Allele Identifier: CA523751864

Gene: DOCK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62513266del , CM000663.2:g.62513266del	GRCh38
NC_000001.10:g.62978937del , CM000663.1:g.62978937del	GRCh37
NC_000001.9:g.62751525del	NCBI36
NG_033073.1:g.180115del
NG_033073.2:g.180115del

Transcript Alleles

HGVS	Amino-acid Change
NM_001367561.1:c.4282+190del MANE Select	NP_001354490.1:n.4282+190del
ENST00000635253.2:c.4282+190del MANE Select	ENSP00000489124.1:n.4282+190del
NM_001271999.1:c.4255+217del	NP_001258928.1:n.4255+217del
NM_001271999.2:c.4255+217del	NP_001258928.1:n.4255+217del
NM_001272000.1:c.4162+217del	NP_001258929.1:n.4162+217del
NM_001272000.2:c.4162+217del	NP_001258929.1:n.4162+217del
NM_001272001.1:c.4162+217del	NP_001258930.1:n.4162+217del
NM_001272001.2:c.4162+217del	NP_001258930.1:n.4162+217del
NM_001330614.1:c.4255+217del	NP_001317543.1:n.4255+217del
NM_001330614.2:c.4255+217del	NP_001317543.1:n.4255+217del
NM_033407.3:c.4189+190del	NP_212132.2:n.4189+190del
NM_033407.4:c.4189+190del	NP_212132.2:n.4189+190del
ENST00000251157.10:c.4255+217del	ENSP00000251157.6:n.4255+217del
ENST00000340370.10:c.4189+190del	ENSP00000340742.5:n.4189+190del
ENST00000454575.6:c.4255+217del	ENSP00000413583.2:n.4255+217del
ENST00000634264.1:c.4162+217del	ENSP00000489284.1:n.4162+217del
ENST00000635123.1:c.4162+217del	ENSP00000489499.1:n.4162+217del
ENST00000635253.1:c.4282+190del	ENSP00000489124.1:n.4282+190del
ENST00000635286.1:n.360+217del
ENST00000637208.1:c.*2375+217del	ENSP00000490079.1:n.*2375+217del
ENST00000637255.1:c.1555+217del	ENSP00000490888.1:n.1555+217del
XM_005271292.1:c.4255+217del	XP_005271349.1:n.4255+217del
XM_011542326.1:c.4282+190del	XP_011540628.1:n.4282+190del
XM_011542326.2:c.4282+190del	XP_011540628.1:n.4282+190del
XM_011542327.1:c.4282+190del	XP_011540629.1:n.4282+190del
XM_011542327.2:c.4282+190del	XP_011540629.1:n.4282+190del
XM_011542328.1:c.4282+190del	XP_011540630.1:n.4282+190del
XM_011542328.2:c.4282+190del	XP_011540630.1:n.4282+190del
XM_011542329.1:c.4282+190del	XP_011540631.1:n.4282+190del
XM_011542330.1:c.4282+190del	XP_011540632.1:n.4282+190del
XM_011542330.2:c.4282+190del	XP_011540632.1:n.4282+190del
XM_017002639.1:c.4189+190del	XP_016858128.1:n.4189+190del
XM_017002640.1:c.4282+190del	XP_016858129.1:n.4282+190del