Canonical Allele Identifier: CA1171093159
Gene: DOCK7 HGNC NCBI

Linked Data

dbSNP Id: rs1645663553

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62465912_62465913insTT , CM000663.2:g.62465912_62465913insTT GRCh38
NC_000001.10:g.62931583_62931584insTT , CM000663.1:g.62931583_62931584insTT GRCh37
NC_000001.9:g.62704171_62704172insTT NCBI36
NG_033073.1:g.227456_227457insAA
NG_033073.2:g.227456_227457insAA

Transcript Alleles

HGVS Amino-acid change
ENST00000634495.2:n.2353+8069_2353+8070insAA
ENST00000635253.2:c.6212+8069_6212+8070insAA MANE Select ENSP00000489124.1:n.6212+8069_6212+8070in...
ENST00000635983.1:n.5891+8069_5891+8070insAA
ENST00000637255.1:c.3479+8069_3479+8070insAA ENSP00000490888.1:n.3479+8069_3479+8070in...
ENST00000637306.1:n.64-4943_64-4942insAA
ENST00000251157.10:c.6185+8069_6185+8070insAA ENSP00000251157.6:n.6185+8069_6185+8070in...
ENST00000340370.10:c.6119+8069_6119+8070insAA ENSP00000340742.5:n.6119+8069_6119+8070in...
ENST00000454575.6:c.6179+8069_6179+8070insAA ENSP00000413583.2:n.6179+8069_6179+8070in...
ENST00000634264.1:c.6092+8069_6092+8070insAA ENSP00000489284.1:n.6092+8069_6092+8070in...
ENST00000634495.1:n.898+8069_898+8070insAA
ENST00000635123.1:c.6086+8069_6086+8070insAA ENSP00000489499.1:n.6086+8069_6086+8070in...
ENST00000635253.1:c.6212+8069_6212+8070insAA ENSP00000489124.1:n.6212+8069_6212+8070in...
NM_001271999.1:c.6179+8069_6179+8070insAA NP_001258928.1:n.6179+8069_6179+8070insAA...
NM_001272000.1:c.6092+8069_6092+8070insAA NP_001258929.1:n.6092+8069_6092+8070insAA...
NM_001272001.1:c.6086+8069_6086+8070insAA NP_001258930.1:n.6086+8069_6086+8070insAA...
NM_033407.3:c.6119+8069_6119+8070insAA NP_212132.2:n.6119+8069_6119+8070insAA
XM_005271292.1:c.6185+8069_6185+8070insAA XP_005271349.1:n.6185+8069_6185+8070insAA...
XM_011542326.1:c.6212+8069_6212+8070insAA XP_011540628.1:n.6212+8069_6212+8070insAA...
XM_011542327.1:c.6206+8069_6206+8070insAA XP_011540629.1:n.6206+8069_6206+8070insAA...
XM_011542328.1:c.6197+8069_6197+8070insAA XP_011540630.1:n.6197+8069_6197+8070insAA...
NM_001330614.1:c.6185+8069_6185+8070insAA NP_001317543.1:n.6185+8069_6185+8070insAA...
XM_011542326.2:c.6212+8069_6212+8070insAA XP_011540628.1:n.6212+8069_6212+8070insAA...
XM_011542327.2:c.6206+8069_6206+8070insAA XP_011540629.1:n.6206+8069_6206+8070insAA...
XM_011542328.2:c.6197+8069_6197+8070insAA XP_011540630.1:n.6197+8069_6197+8070insAA...
XM_017002639.1:c.6113+8069_6113+8070insAA XP_016858128.1:n.6113+8069_6113+8070insAA...
NM_001367561.1:c.6212+8069_6212+8070insAA MANE Select NP_001354490.1:n.6212+8069_6212+8070insAA...
NM_001271999.2:c.6179+8069_6179+8070insAA NP_001258928.1:n.6179+8069_6179+8070insAA...
NM_001272000.2:c.6092+8069_6092+8070insAA NP_001258929.1:n.6092+8069_6092+8070insAA...
NM_001272001.2:c.6086+8069_6086+8070insAA NP_001258930.1:n.6086+8069_6086+8070insAA...
NM_001330614.2:c.6185+8069_6185+8070insAA NP_001317543.1:n.6185+8069_6185+8070insAA...
NM_033407.4:c.6119+8069_6119+8070insAA NP_212132.2:n.6119+8069_6119+8070insAA