Canonical Allele Identifier: CA885370
Gene: DOCK7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62476098G>C , CM000663.2:g.62476098G>C GRCh38
NC_000001.10:g.62941769G>C , CM000663.1:g.62941769G>C GRCh37
NC_000001.9:g.62714357G>C NCBI36
NG_033073.1:g.217271C>G
NG_033073.2:g.217271C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000634495.2:n.1834C>G
ENST00000635253.2:c.5693C>G MANE Select ENSP00000489124.1:p.Pro1898Arg
ENST00000635983.1:n.5372C>G
ENST00000637255.1:c.2960C>G ENSP00000490888.1:p.Pro987Arg
ENST00000637487.1:n.96C>G
ENST00000251157.10:c.5666C>G ENSP00000251157.6:p.Pro1889Arg
ENST00000340370.10:c.5600C>G ENSP00000340742.5:p.Pro1867Arg
ENST00000454575.6:c.5660C>G ENSP00000413583.2:p.Pro1887Arg
ENST00000467758.1:n.92C>G
ENST00000489185.1:n.1364C>G
ENST00000634264.1:c.5573C>G ENSP00000489284.1:p.Pro1858Arg
ENST00000634495.1:n.379C>G
ENST00000635123.1:c.5567C>G ENSP00000489499.1:p.Pro1856Arg
ENST00000635253.1:c.5693C>G ENSP00000489124.1:p.Pro1898Arg
NM_001271999.1:c.5660C>G NP_001258928.1:p.Pro1887Arg
NM_001272000.1:c.5573C>G NP_001258929.1:p.Pro1858Arg
NM_001272001.1:c.5567C>G NP_001258930.1:p.Pro1856Arg
NM_033407.3:c.5600C>G NP_212132.2:p.Pro1867Arg
XM_005271292.1:c.5666C>G XP_005271349.1:p.Pro1889Arg
XM_011542326.1:c.5693C>G XP_011540628.1:p.Pro1898Arg
XM_011542327.1:c.5687C>G XP_011540629.1:p.Pro1896Arg
XM_011542328.1:c.5678C>G XP_011540630.1:p.Pro1893Arg
NM_001330614.1:c.5666C>G NP_001317543.1:p.Pro1889Arg
XM_011542326.2:c.5693C>G XP_011540628.1:p.Pro1898Arg
XM_011542327.2:c.5687C>G XP_011540629.1:p.Pro1896Arg
XM_011542328.2:c.5678C>G XP_011540630.1:p.Pro1893Arg
XM_017002639.1:c.5594C>G XP_016858128.1:p.Pro1865Arg
NM_001367561.1:c.5693C>G MANE Select NP_001354490.1:p.Pro1898Arg
NM_001271999.2:c.5660C>G NP_001258928.1:p.Pro1887Arg
NM_001272000.2:c.5573C>G NP_001258929.1:p.Pro1858Arg
NM_001272001.2:c.5567C>G NP_001258930.1:p.Pro1856Arg
NM_001330614.2:c.5666C>G NP_001317543.1:p.Pro1889Arg
NM_033407.4:c.5600C>G NP_212132.2:p.Pro1867Arg