Canonical Allele Identifier: CA1171146712

Gene: DOCK7

Linked Data

• dbSNP Id: rs1649414395
• gnomAD v4: 1-62597398-GGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62597403_62597405del , CM000663.2:g.62597403_62597405del	GRCh38
NC_000001.10:g.63063074_63063076del , CM000663.1:g.63063074_63063076del	GRCh37
NC_000001.9:g.62835662_62835664del	NCBI36
NG_028169.1:g.4888_4890del
NG_033073.1:g.95968_95970del
NG_033073.2:g.95968_95970del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614472.5:c.1389-10777_1389-10775del	ENSP00000483062.2:n.1389-10777_1389-10775del
ENST00000635253.2:c.1683-10777_1683-10775del MANE Select	ENSP00000489124.1:n.1683-10777_1683-10775del
ENST00000637208.1:c.1683-10777_1683-10775del	ENSP00000490079.1:n.1683-10777_1683-10775del
ENST00000251157.10:c.1683-10777_1683-10775del	ENSP00000251157.6:n.1683-10777_1683-10775del
ENST00000340370.10:c.1683-10777_1683-10775del	ENSP00000340742.5:n.1683-10777_1683-10775del
ENST00000404627.3:c.1683-10777_1683-10775del	ENSP00000384446.2:n.1683-10777_1683-10775del
ENST00000454575.6:c.1683-10777_1683-10775del	ENSP00000413583.2:n.1683-10777_1683-10775del
ENST00000614472.4:c.1359-10777_1359-10775del	ENSP00000483062.1:n.1359-10777_1359-10775del
ENST00000634223.1:c.13-10777_13-10775del
ENST00000634264.1:c.1683-10777_1683-10775del	ENSP00000489284.1:n.1683-10777_1683-10775del
ENST00000635123.1:c.1683-10777_1683-10775del	ENSP00000489499.1:n.1683-10777_1683-10775del
ENST00000635253.1:c.1683-10777_1683-10775del	ENSP00000489124.1:n.1683-10777_1683-10775del
NM_001271999.1:c.1683-10777_1683-10775del	NP_001258928.1:n.1683-10777_1683-10775del
NM_001272000.1:c.1683-10777_1683-10775del	NP_001258929.1:n.1683-10777_1683-10775del
NM_001272001.1:c.1683-10777_1683-10775del	NP_001258930.1:n.1683-10777_1683-10775del
NM_001272002.1:c.1683-10777_1683-10775del	NP_001258931.1:n.1683-10777_1683-10775del
NM_033407.3:c.1683-10777_1683-10775del	NP_212132.2:n.1683-10777_1683-10775del
XM_005271292.1:c.1683-10777_1683-10775del	XP_005271349.1:n.1683-10777_1683-10775del
XM_011542326.1:c.1683-10777_1683-10775del	XP_011540628.1:n.1683-10777_1683-10775del
XM_011542327.1:c.1683-10777_1683-10775del	XP_011540629.1:n.1683-10777_1683-10775del
XM_011542328.1:c.1683-10777_1683-10775del	XP_011540630.1:n.1683-10777_1683-10775del
XM_011542329.1:c.1683-10777_1683-10775del	XP_011540631.1:n.1683-10777_1683-10775del
XM_011542330.1:c.1683-10777_1683-10775del	XP_011540632.1:n.1683-10777_1683-10775del
NM_001330614.1:c.1683-10777_1683-10775del	NP_001317543.1:n.1683-10777_1683-10775del
XM_011542326.2:c.1683-10777_1683-10775del	XP_011540628.1:n.1683-10777_1683-10775del
XM_011542327.2:c.1683-10777_1683-10775del	XP_011540629.1:n.1683-10777_1683-10775del
XM_011542328.2:c.1683-10777_1683-10775del	XP_011540630.1:n.1683-10777_1683-10775del
XM_011542330.2:c.1683-10777_1683-10775del	XP_011540632.1:n.1683-10777_1683-10775del
XM_017002639.1:c.1683-10777_1683-10775del	XP_016858128.1:n.1683-10777_1683-10775del
XM_017002640.1:c.1683-10777_1683-10775del	XP_016858129.1:n.1683-10777_1683-10775del
NM_001367561.1:c.1683-10777_1683-10775del MANE Select	NP_001354490.1:n.1683-10777_1683-10775del
NM_001272002.2:c.1683-10777_1683-10775del	NP_001258931.1:n.1683-10777_1683-10775del
NM_001271999.2:c.1683-10777_1683-10775del	NP_001258928.1:n.1683-10777_1683-10775del
NM_001272000.2:c.1683-10777_1683-10775del	NP_001258929.1:n.1683-10777_1683-10775del
NM_001272001.2:c.1683-10777_1683-10775del	NP_001258930.1:n.1683-10777_1683-10775del
NM_001330614.2:c.1683-10777_1683-10775del	NP_001317543.1:n.1683-10777_1683-10775del
NM_033407.4:c.1683-10777_1683-10775del	NP_212132.2:n.1683-10777_1683-10775del