Canonical Allele Identifier: CA2159619938
Gene: DYNC1H1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102048415G= , CM000676.2:g.102048415G= GRCh38
NC_000014.8:g.102514752G= , CM000676.1:g.102514752G= GRCh37
NC_000014.7:g.101584505G= NCBI36
NG_008777.1:g.88888G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684561.1:c.*4678-101G= ENSP00000506816.1:n.*4678-101G=
ENST00000360184.10:c.13219-101G= MANE Select ENSP00000348965.4:n.13219-101G=
ENST00000553701.1:n.346+2030C=
ENST00000555062.2:n.292-101G=
ENST00000556229.2:n.612-101G=
ENST00000557242.1:n.328+4112C=
ENST00000643437.1:n.3173-101G=
ENST00000643591.1:n.1012-101G=
ENST00000643729.1:n.751G=
ENST00000643829.1:n.3175-101G=
ENST00000644239.2:n.1355-101G=
ENST00000644794.1:n.3724G=
ENST00000644881.2:c.13219-101G= ENSP00000495022.2:n.13219-101G=
ENST00000645039.2:c.*1070-101G= ENSP00000495220.2:n.*1070-101G=
ENST00000645085.1:n.1465-101G=
ENST00000645149.2:c.13072-101G= ENSP00000495944.2:n.13072-101G=
ENST00000647143.1:n.753G=
ENST00000647204.2:n.2555-101G=
ENST00000647366.1:n.6773-101G=
ENST00000679720.1:c.13219-101G= ENSP00000505938.1:n.13219-101G=
ENST00000679910.1:c.*4301-101G= ENSP00000506521.1:n.*4301-101G=
ENST00000680120.1:c.13219-115G= ENSP00000504863.1:n.13219-115G=
ENST00000680178.1:n.677G=
ENST00000680200.1:c.*2478-101G= ENSP00000506166.1:n.*2478-101G=
ENST00000680313.1:c.13219-101G= ENSP00000506208.1:n.13219-101G=
ENST00000680423.1:c.*4950-101G= ENSP00000505483.1:n.*4950-101G=
ENST00000680715.1:c.*509-101G= ENSP00000505332.1:n.*509-101G=
ENST00000681066.1:c.*1242-101G= ENSP00000506344.1:n.*1242-101G=
ENST00000681283.1:c.*1931-101G= ENSP00000505667.1:n.*1931-101G=
ENST00000681536.1:c.*6418-101G= ENSP00000505821.1:n.*6418-101G=
ENST00000681574.1:c.13219-101G= ENSP00000505523.1:n.13219-101G=
ENST00000681822.1:c.13219-101G= ENSP00000505744.1:n.13219-101G=
ENST00000360184.8:c.13219-101G= ENSP00000348965.4:n.13219-101G=
ENST00000555062.1:n.269-101G=
ENST00000556229.1:n.369-101G=
NM_001376.4:c.13219-101G= NP_001367.2:n.13219-101G=
NM_001376.5:c.13219-101G= MANE Select NP_001367.2:n.13219-101G=