Canonical Allele Identifier: CA1140212418

Gene: DOCK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62652525A= , CM000663.2:g.62652525A=	GRCh38
NC_000001.10:g.63118196A= , CM000663.1:g.63118196A=	GRCh37
NC_000001.9:g.62890784A=	NCBI36
NG_033073.1:g.40844T=
NG_033073.2:g.40844T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614472.5:c.59+1200T=	ENSP00000483062.2:n.59+1200T=
ENST00000635253.2:c.389+1200T= MANE Select	ENSP00000489124.1:n.389+1200T=
ENST00000635827.1:c.327+1200T=
ENST00000637208.1:c.389+1200T=	ENSP00000490079.1:n.389+1200T=
ENST00000251157.10:c.389+1200T=	ENSP00000251157.6:n.389+1200T=
ENST00000340370.10:c.389+1200T=	ENSP00000340742.5:n.389+1200T=
ENST00000404627.3:c.389+1200T=	ENSP00000384446.2:n.389+1200T=
ENST00000454575.6:c.389+1200T=	ENSP00000413583.2:n.389+1200T=
ENST00000614472.4:c.65+1200T=	ENSP00000483062.1:n.65+1200T=
ENST00000634264.1:c.389+1200T=	ENSP00000489284.1:n.389+1200T=
ENST00000635123.1:c.389+1200T=	ENSP00000489499.1:n.389+1200T=
ENST00000635253.1:c.389+1200T=	ENSP00000489124.1:n.389+1200T=
NM_001271999.1:c.389+1200T=	NP_001258928.1:n.389+1200T=
NM_001272000.1:c.389+1200T=	NP_001258929.1:n.389+1200T=
NM_001272001.1:c.389+1200T=	NP_001258930.1:n.389+1200T=
NM_001272002.1:c.389+1200T=	NP_001258931.1:n.389+1200T=
NM_033407.3:c.389+1200T=	NP_212132.2:n.389+1200T=
XM_005271292.1:c.389+1200T=	XP_005271349.1:n.389+1200T=
XM_011542326.1:c.389+1200T=	XP_011540628.1:n.389+1200T=
XM_011542327.1:c.389+1200T=	XP_011540629.1:n.389+1200T=
XM_011542328.1:c.389+1200T=	XP_011540630.1:n.389+1200T=
XM_011542329.1:c.389+1200T=	XP_011540631.1:n.389+1200T=
XM_011542330.1:c.389+1200T=	XP_011540632.1:n.389+1200T=
NM_001330614.1:c.389+1200T=	NP_001317543.1:n.389+1200T=
XM_011542326.2:c.389+1200T=	XP_011540628.1:n.389+1200T=
XM_011542327.2:c.389+1200T=	XP_011540629.1:n.389+1200T=
XM_011542328.2:c.389+1200T=	XP_011540630.1:n.389+1200T=
XM_011542330.2:c.389+1200T=	XP_011540632.1:n.389+1200T=
XM_017002639.1:c.389+1200T=	XP_016858128.1:n.389+1200T=
XM_017002640.1:c.389+1200T=	XP_016858129.1:n.389+1200T=
NM_001367561.1:c.389+1200T= MANE Select	NP_001354490.1:n.389+1200T=
NM_001272002.2:c.389+1200T=	NP_001258931.1:n.389+1200T=
NM_001271999.2:c.389+1200T=	NP_001258928.1:n.389+1200T=
NM_001272000.2:c.389+1200T=	NP_001258929.1:n.389+1200T=
NM_001272001.2:c.389+1200T=	NP_001258930.1:n.389+1200T=
NM_001330614.2:c.389+1200T=	NP_001317543.1:n.389+1200T=
NM_033407.4:c.389+1200T=	NP_212132.2:n.389+1200T=