Canonical Allele Identifier: CA737703736

Gene: DOCK7

Linked Data

• dbSNP Id: rs1320537126
• gnomAD v3: 1-62465795-C-CTG
• gnomAD v4: 1-62465795-C-CTG
• MyVariant Identifiers: chr1:g.62931466_62931467insTG (hg19) ; chr1:g.62465795_62465796insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62465797_62465798dup , CM000663.2:g.62465797_62465798dup	GRCh38
NC_000001.10:g.62931468_62931469dup , CM000663.1:g.62931468_62931469dup	GRCh37
NC_000001.9:g.62704056_62704057dup	NCBI36
NG_033073.1:g.227572_227573dup
NG_033073.2:g.227572_227573dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000634495.2:n.2354-8092_2354-8091dup
ENST00000635253.2:c.6213-8092_6213-8091dup MANE Select	ENSP00000489124.1:n.6213-8092_6213-8091dup
ENST00000635983.1:n.5892-8092_5892-8091dup
ENST00000637255.1:c.3480-8092_3480-8091dup	ENSP00000490888.1:n.3480-8092_3480-8091dup
ENST00000637306.1:n.64-4827_64-4826dup
ENST00000251157.10:c.6186-8092_6186-8091dup	ENSP00000251157.6:n.6186-8092_6186-8091dup
ENST00000340370.10:c.6120-8092_6120-8091dup	ENSP00000340742.5:n.6120-8092_6120-8091dup
ENST00000454575.6:c.6180-8092_6180-8091dup	ENSP00000413583.2:n.6180-8092_6180-8091dup
ENST00000634264.1:c.6093-8092_6093-8091dup	ENSP00000489284.1:n.6093-8092_6093-8091dup
ENST00000634495.1:n.899-8092_899-8091dup
ENST00000635123.1:c.6087-8092_6087-8091dup	ENSP00000489499.1:n.6087-8092_6087-8091dup
ENST00000635253.1:c.6213-8092_6213-8091dup	ENSP00000489124.1:n.6213-8092_6213-8091dup
NM_001271999.1:c.6180-8092_6180-8091dup	NP_001258928.1:n.6180-8092_6180-8091dup
NM_001272000.1:c.6093-8092_6093-8091dup	NP_001258929.1:n.6093-8092_6093-8091dup
NM_001272001.1:c.6087-8092_6087-8091dup	NP_001258930.1:n.6087-8092_6087-8091dup
NM_033407.3:c.6120-8092_6120-8091dup	NP_212132.2:n.6120-8092_6120-8091dup
XM_005271292.1:c.6186-8092_6186-8091dup	XP_005271349.1:n.6186-8092_6186-8091dup
XM_011542326.1:c.6213-8092_6213-8091dup	XP_011540628.1:n.6213-8092_6213-8091dup
XM_011542327.1:c.6207-8092_6207-8091dup	XP_011540629.1:n.6207-8092_6207-8091dup
XM_011542328.1:c.6198-8092_6198-8091dup	XP_011540630.1:n.6198-8092_6198-8091dup
NM_001330614.1:c.6186-8092_6186-8091dup	NP_001317543.1:n.6186-8092_6186-8091dup
XM_011542326.2:c.6213-8092_6213-8091dup	XP_011540628.1:n.6213-8092_6213-8091dup
XM_011542327.2:c.6207-8092_6207-8091dup	XP_011540629.1:n.6207-8092_6207-8091dup
XM_011542328.2:c.6198-8092_6198-8091dup	XP_011540630.1:n.6198-8092_6198-8091dup
XM_017002639.1:c.6114-8092_6114-8091dup	XP_016858128.1:n.6114-8092_6114-8091dup
NM_001367561.1:c.6213-8092_6213-8091dup MANE Select	NP_001354490.1:n.6213-8092_6213-8091dup
NM_001271999.2:c.6180-8092_6180-8091dup	NP_001258928.1:n.6180-8092_6180-8091dup
NM_001272000.2:c.6093-8092_6093-8091dup	NP_001258929.1:n.6093-8092_6093-8091dup
NM_001272001.2:c.6087-8092_6087-8091dup	NP_001258930.1:n.6087-8092_6087-8091dup
NM_001330614.2:c.6186-8092_6186-8091dup	NP_001317543.1:n.6186-8092_6186-8091dup
NM_033407.4:c.6120-8092_6120-8091dup	NP_212132.2:n.6120-8092_6120-8091dup