Canonical Allele Identifier: CA13174038
Gene: DOCK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.126979126G>C , CM000672.2:g.126979126G>C GRCh38
NC_000010.10:g.128777390G>C , CM000672.1:g.128777390G>C GRCh37
NC_000010.9:g.128667380G>C NCBI36
NG_033919.1:g.78673G>C
NG_033919.2:g.78673G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000623213.2:c.171+1138G>C MANE Select ENSP00000485033.1:n.171+1138G>C
ENST00000280333.9:c.171+1138G>C ENSP00000280333.6:n.171+1138G>C
ENST00000623213.1:c.171+1138G>C ENSP00000485033.1:n.171+1138G>C
NM_001290223.1:c.171+1138G>C NP_001277152.1:n.171+1138G>C
NM_001380.4:c.171+1138G>C NP_001371.1:n.171+1138G>C
XM_011539421.1:c.288+1138G>C XP_011537723.1:n.288+1138G>C
XM_011539422.1:c.237+1138G>C XP_011537724.1:n.237+1138G>C
XM_011539423.1:c.288+1138G>C XP_011537725.1:n.288+1138G>C
XM_011539424.1:c.153+1138G>C XP_011537726.1:n.153+1138G>C
XM_011539425.1:c.288+1138G>C XP_011537727.1:n.288+1138G>C
XM_011539426.1:c.288+1138G>C XP_011537728.1:n.288+1138G>C
XM_011539422.3:c.237+1138G>C XP_011537724.1:n.237+1138G>C
XM_017015813.2:c.237+1138G>C XP_016871302.1:n.237+1138G>C
XM_017015814.1:c.237+1138G>C XP_016871303.1:n.237+1138G>C
XM_017015815.1:c.171+1138G>C XP_016871304.1:n.171+1138G>C
XM_017015817.1:c.237+1138G>C XP_016871306.1:n.237+1138G>C
NM_001290223.2:c.171+1138G>C MANE Select NP_001277152.2:n.171+1138G>C
NM_001377543.1:c.171+1138G>C NP_001364472.1:n.171+1138G>C
NM_001377544.1:c.207+1138G>C NP_001364473.1:n.207+1138G>C
NM_001377546.1:c.171+1138G>C NP_001364475.1:n.171+1138G>C
NM_001377547.1:c.171+1138G>C NP_001364476.1:n.171+1138G>C
NM_001377548.1:c.87+1138G>C NP_001364477.1:n.87+1138G>C
NM_001377550.1:c.171+1138G>C NP_001364479.1:n.171+1138G>C
NM_001377553.1:c.171+1138G>C NP_001364482.1:n.171+1138G>C
NM_001377554.1:c.171+1138G>C NP_001364483.1:n.171+1138G>C
NM_001377556.1:c.171+1138G>C NP_001364485.1:n.171+1138G>C
NM_001377558.1:c.171+1138G>C NP_001364487.1:n.171+1138G>C
NM_001377560.1:c.130+8341G>C NP_001364489.1:n.130+8341G>C
NM_001377561.1:c.171+1138G>C NP_001364490.1:n.171+1138G>C
NM_001380.5:c.171+1138G>C NP_001371.2:n.171+1138G>C