Canonical Allele Identifier: CA16055259
Gene: DOCK7 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1167998

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.62465961C>A , CM000663.2:g.62465961C>A GRCh38
NC_000001.10:g.62931632C>A , CM000663.1:g.62931632C>A GRCh37
NC_000001.9:g.62704220C>A NCBI36
NG_033073.1:g.227408G>T

Transcript Alleles

HGVS Amino-acid change
NM_001271999.1:c.6179+8021G>T VV NP_001258928.1:p.=
NM_001272000.1:c.6092+8021G>T VV NP_001258929.1:p.=
NM_001272001.1:c.6086+8021G>T VV NP_001258930.1:p.=
NM_033407.3:c.6119+8021G>T VV NP_212132.2:p.=
XM_005271292.1:c.6185+8021G>T XP_005271349.1:p.=
XM_011542326.1:c.6212+8021G>T XP_011540628.1:p.=
XM_011542327.1:c.6206+8021G>T XP_011540629.1:p.=
XM_011542328.1:c.6197+8021G>T XP_011540630.1:p.=
NM_001330614.1:c.6185+8021G>T VV NP_001317543.1:p.=
XM_011542326.2:c.6212+8021G>T
XM_011542327.2:c.6206+8021G>T
XM_011542328.2:c.6197+8021G>T
XM_017002639.1:c.6113+8021G>T XP_016858128.1:p.=
ENST00000251157.10:n.6185+8021G>T ENSP00000251157.6:p.=
ENST00000340370.10:n.6119+8021G>T ENSP00000340742.5:p.=
ENST00000454575.6:c.6179+8021G>T ENSP00000413583.2:p.=
ENST00000634264.1:n.6092+8021G>T ENSP00000489284.1:p.=
ENST00000634495.1:n.898+8021G>T
ENST00000635123.1:n.6086+8021G>T ENSP00000489499.1:p.=
ENST00000635253.1:n.6212+8021G>T ENSP00000489124.1:p.=