Canonical Allele Identifier: CA340604539

Gene: DOCK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62476107T>G , CM000663.2:g.62476107T>G	GRCh38
NC_000001.10:g.62941778T>G , CM000663.1:g.62941778T>G	GRCh37
NC_000001.9:g.62714366T>G	NCBI36
NG_033073.1:g.217262A>C
NG_033073.2:g.217262A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634495.2:n.1825A>C
ENST00000635253.2:c.5684A>C MANE Select	ENSP00000489124.1:p.Asp1895Ala
ENST00000635983.1:n.5363A>C
ENST00000637255.1:c.2951A>C	ENSP00000490888.1:p.Asp984Ala
ENST00000637487.1:n.87A>C
ENST00000251157.10:c.5657A>C	ENSP00000251157.6:p.Asp1886Ala
ENST00000340370.10:c.5591A>C	ENSP00000340742.5:p.Asp1864Ala
ENST00000454575.6:c.5651A>C	ENSP00000413583.2:p.Asp1884Ala
ENST00000467758.1:n.83A>C
ENST00000489185.1:n.1355A>C
ENST00000634264.1:c.5564A>C	ENSP00000489284.1:p.Asp1855Ala
ENST00000634495.1:n.370A>C
ENST00000635123.1:c.5558A>C	ENSP00000489499.1:p.Asp1853Ala
ENST00000635253.1:c.5684A>C	ENSP00000489124.1:p.Asp1895Ala
NM_001271999.1:c.5651A>C	NP_001258928.1:p.Asp1884Ala
NM_001272000.1:c.5564A>C	NP_001258929.1:p.Asp1855Ala
NM_001272001.1:c.5558A>C	NP_001258930.1:p.Asp1853Ala
NM_033407.3:c.5591A>C	NP_212132.2:p.Asp1864Ala
XM_005271292.1:c.5657A>C	XP_005271349.1:p.Asp1886Ala
XM_011542326.1:c.5684A>C	XP_011540628.1:p.Asp1895Ala
XM_011542327.1:c.5678A>C	XP_011540629.1:p.Asp1893Ala
XM_011542328.1:c.5669A>C	XP_011540630.1:p.Asp1890Ala
NM_001330614.1:c.5657A>C	NP_001317543.1:p.Asp1886Ala
XM_011542326.2:c.5684A>C	XP_011540628.1:p.Asp1895Ala
XM_011542327.2:c.5678A>C	XP_011540629.1:p.Asp1893Ala
XM_011542328.2:c.5669A>C	XP_011540630.1:p.Asp1890Ala
XM_017002639.1:c.5585A>C	XP_016858128.1:p.Asp1862Ala
NM_001367561.1:c.5684A>C MANE Select	NP_001354490.1:p.Asp1895Ala
NM_001271999.2:c.5651A>C	NP_001258928.1:p.Asp1884Ala
NM_001272000.2:c.5564A>C	NP_001258929.1:p.Asp1855Ala
NM_001272001.2:c.5558A>C	NP_001258930.1:p.Asp1853Ala
NM_001330614.2:c.5657A>C	NP_001317543.1:p.Asp1886Ala
NM_033407.4:c.5591A>C	NP_212132.2:p.Asp1864Ala