Canonical Allele Identifier: CA2159623080
Gene: DYNC1H1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102039668C= , CM000676.2:g.102039668C= GRCh38
NC_000014.8:g.102506005C= , CM000676.1:g.102506005C= GRCh37
NC_000014.7:g.101575758C= NCBI36
NG_008777.1:g.80141C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684561.1:c.*3085C= ENSP00000506816.1:n.*3085C=
ENST00000360184.10:c.11626C= MANE Select ENSP00000348965.4:p.Leu3876=
ENST00000553701.1:n.347-2899G=
ENST00000556139.2:n.178C=
ENST00000557242.1:n.329-2899G=
ENST00000557551.1:n.112-2899G=
ENST00000643437.1:n.1580C=
ENST00000643829.1:n.1455C=
ENST00000644794.1:n.1745C=
ENST00000644881.2:c.11626C= ENSP00000495022.2:p.Leu3876=
ENST00000645039.2:c.11626C= ENSP00000495220.2:p.Leu3876=
ENST00000645085.1:n.123C=
ENST00000645149.2:c.11479C= ENSP00000495944.2:p.Leu3827=
ENST00000645697.1:n.2289C=
ENST00000647204.2:n.867C=
ENST00000647366.1:n.5180C=
ENST00000679486.1:c.11626C= ENSP00000506688.1:p.Leu3876=
ENST00000679629.1:c.11626C= ENSP00000505589.1:p.Leu3876=
ENST00000679720.1:c.11626C= ENSP00000505938.1:p.Leu3876=
ENST00000679910.1:c.*2708C= ENSP00000506521.1:n.*2708C=
ENST00000680120.1:c.11626C= ENSP00000504863.1:p.Leu3876=
ENST00000680200.1:c.*885C= ENSP00000506166.1:n.*885C=
ENST00000680313.1:c.11626C= ENSP00000506208.1:p.Leu3876=
ENST00000680423.1:c.*3357C= ENSP00000505483.1:n.*3357C=
ENST00000680715.1:c.11626C= ENSP00000505332.1:p.Leu3876=
ENST00000681010.1:c.11626C= ENSP00000505201.1:p.Leu3876=
ENST00000681066.1:c.11626C= ENSP00000506344.1:p.Leu3876=
ENST00000681123.1:c.11626C= ENSP00000506124.1:p.Leu3876=
ENST00000681283.1:c.*338C= ENSP00000505667.1:n.*338C=
ENST00000681536.1:c.*4825C= ENSP00000505821.1:n.*4825C=
ENST00000681574.1:c.11626C= ENSP00000505523.1:p.Leu3876=
ENST00000681822.1:c.11626C= ENSP00000505744.1:p.Leu3876=
ENST00000360184.8:c.11626C= ENSP00000348965.4:p.Leu3876=
ENST00000556139.1:n.178C=
NM_001376.4:c.11626C= NP_001367.2:p.Leu3876=
NM_001376.5:c.11626C= MANE Select NP_001367.2:p.Leu3876=