Canonical Allele Identifier: CA885175

Gene: DOCK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62455259G>A , CM000663.2:g.62455259G>A	GRCh38
NC_000001.10:g.62920930G>A , CM000663.1:g.62920930G>A	GRCh37
NC_000001.9:g.62693518G>A	NCBI36
NG_033073.1:g.238110C>T
NG_033073.2:g.238110C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001367561.1:c.*155C>T MANE Select	NP_001354490.1:n.*155C>T
ENST00000635253.2:c.*155C>T MANE Select	ENSP00000489124.1:n.*155C>T
NM_001271999.1:c.*155C>T	NP_001258928.1:n.*155C>T
NM_001271999.2:c.*155C>T	NP_001258928.1:n.*155C>T
NM_001272000.1:c.*155C>T	NP_001258929.1:n.*155C>T
NM_001272000.2:c.*155C>T	NP_001258929.1:n.*155C>T
NM_001272001.1:c.*155C>T	NP_001258930.1:n.*155C>T
NM_001272001.2:c.*155C>T	NP_001258930.1:n.*155C>T
NM_001330614.1:c.*155C>T	NP_001317543.1:n.*155C>T
NM_001330614.2:c.*155C>T	NP_001317543.1:n.*155C>T
NM_033407.3:c.*155C>T	NP_212132.2:n.*155C>T
NM_033407.4:c.*155C>T	NP_212132.2:n.*155C>T
ENST00000251157.10:c.6551C>T	ENSP00000251157.6:n.6551C>T
ENST00000340370.10:c.6485C>T	ENSP00000340742.5:n.6485C>T
ENST00000454575.6:c.*155C>T	ENSP00000413583.2:n.*155C>T
ENST00000634495.1:n.1264C>T
ENST00000634495.2:n.2717C>T
ENST00000635348.1:n.1860C>T
ENST00000635983.1:n.6257C>T
ENST00000637255.1:c.3845C>T	ENSP00000490888.1:n.3845C>T
XM_005271292.1:c.*155C>T	XP_005271349.1:n.*155C>T
XM_011542326.1:c.*155C>T	XP_011540628.1:n.*155C>T
XM_011542326.2:c.*155C>T	XP_011540628.1:n.*155C>T
XM_011542327.1:c.*155C>T	XP_011540629.1:n.*155C>T
XM_011542327.2:c.*155C>T	XP_011540629.1:n.*155C>T
XM_011542328.1:c.*155C>T	XP_011540630.1:n.*155C>T
XM_011542328.2:c.*155C>T	XP_011540630.1:n.*155C>T
XM_017002639.1:c.*155C>T	XP_016858128.1:n.*155C>T