Canonical Allele Identifier: CA2159622999

Gene: DYNC1H1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102039608_102039611delinsGAAC , CM000676.2:g.102039608_102039611delinsGAAC	GRCh38
NC_000014.8:g.102505945_102505948delinsGAAC , CM000676.1:g.102505945_102505948delinsGAAC	GRCh37
NC_000014.7:g.101575698_101575701delinsGAAC	NCBI36
NG_008777.1:g.80081_80084delinsGAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684561.1:c.*3055-30_*3055-27delinsGAAC	ENSP00000506816.1:n.*3055-30_*3055-27delinsGAAC
ENST00000360184.10:c.11596-30_11596-27delinsGAAC MANE Select	ENSP00000348965.4:n.11596-30_11596-27delinsGAAC
ENST00000553701.1:n.347-2842_347-2839delinsGTTC
ENST00000556139.2:n.118_121delinsGAAC
ENST00000557242.1:n.329-2842_329-2839delinsGTTC
ENST00000557551.1:n.112-2842_112-2839delinsGTTC
ENST00000643437.1:n.1550-30_1550-27delinsGAAC
ENST00000643829.1:n.1425-30_1425-27delinsGAAC
ENST00000644794.1:n.1715-30_1715-27delinsGAAC
ENST00000644881.2:c.11596-30_11596-27delinsGAAC	ENSP00000495022.2:n.11596-30_11596-27delinsGAAC
ENST00000645039.2:c.11596-30_11596-27delinsGAAC	ENSP00000495220.2:n.11596-30_11596-27delinsGAAC
ENST00000645085.1:n.63_66delinsGAAC
ENST00000645149.2:c.11449-30_11449-27delinsGAAC	ENSP00000495944.2:n.11449-30_11449-27delinsGAAC
ENST00000645697.1:n.2259-30_2259-27delinsGAAC
ENST00000647204.2:n.837-30_837-27delinsGAAC
ENST00000647366.1:n.5150-30_5150-27delinsGAAC
ENST00000679486.1:c.11596-30_11596-27delinsGAAC	ENSP00000506688.1:n.11596-30_11596-27delinsGAAC
ENST00000679629.1:c.11596-30_11596-27delinsGAAC	ENSP00000505589.1:n.11596-30_11596-27delinsGAAC
ENST00000679720.1:c.11596-30_11596-27delinsGAAC	ENSP00000505938.1:n.11596-30_11596-27delinsGAAC
ENST00000679910.1:c.*2678-30_*2678-27delinsGAAC	ENSP00000506521.1:n.*2678-30_*2678-27delinsGAAC
ENST00000680120.1:c.11596-30_11596-27delinsGAAC	ENSP00000504863.1:n.11596-30_11596-27delinsGAAC
ENST00000680200.1:c.*855-30_*855-27delinsGAAC	ENSP00000506166.1:n.*855-30_*855-27delinsGAAC
ENST00000680313.1:c.11596-30_11596-27delinsGAAC	ENSP00000506208.1:n.11596-30_11596-27delinsGAAC
ENST00000680423.1:c.*3327-30_*3327-27delinsGAAC	ENSP00000505483.1:n.*3327-30_*3327-27delinsGAAC
ENST00000680715.1:c.11596-30_11596-27delinsGAAC	ENSP00000505332.1:n.11596-30_11596-27delinsGAAC
ENST00000681010.1:c.11596-30_11596-27delinsGAAC	ENSP00000505201.1:n.11596-30_11596-27delinsGAAC
ENST00000681066.1:c.11596-30_11596-27delinsGAAC	ENSP00000506344.1:n.11596-30_11596-27delinsGAAC
ENST00000681123.1:c.11596-30_11596-27delinsGAAC	ENSP00000506124.1:n.11596-30_11596-27delinsGAAC
ENST00000681283.1:c.*308-30_*308-27delinsGAAC	ENSP00000505667.1:n.*308-30_*308-27delinsGAAC
ENST00000681536.1:c.*4795-30_*4795-27delinsGAAC	ENSP00000505821.1:n.*4795-30_*4795-27delinsGAAC
ENST00000681574.1:c.11596-30_11596-27delinsGAAC	ENSP00000505523.1:n.11596-30_11596-27delinsGAAC
ENST00000681822.1:c.11596-30_11596-27delinsGAAC	ENSP00000505744.1:n.11596-30_11596-27delinsGAAC
ENST00000360184.8:c.11596-30_11596-27delinsGAAC	ENSP00000348965.4:n.11596-30_11596-27delinsGAAC
ENST00000556139.1:n.118_121delinsGAAC
NM_001376.4:c.11596-30_11596-27delinsGAAC	NP_001367.2:n.11596-30_11596-27delinsGAAC
NM_001376.5:c.11596-30_11596-27delinsGAAC MANE Select	NP_001367.2:n.11596-30_11596-27delinsGAAC