Canonical Allele Identifier: CA206008
Gene: DYNC1H1 HGNC NCBI

Linked Data

ClinVar Variation Id: 210868
dbSNP Id: rs199763298

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.101988697C>T , CM000676.2:g.101988697C>T GRCh38
NC_000014.8:g.102455034C>T , CM000676.1:g.102455034C>T GRCh37
NC_000014.7:g.101524787C>T NCBI36
NG_008777.1:g.29170C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360184.10:c.2719-6C>T MANE Select ENSP00000348965.4:p.=
ENST00000643508.2:c.2719-6C>T ENSP00000495528.2:p.=
ENST00000643684.1:n.2838-6C>T
ENST00000643958.2:c.2719-6C>T ENSP00000505734.1:p.=
ENST00000644881.2:c.2719-6C>T ENSP00000495022.2:p.=
ENST00000645039.2:c.2719-6C>T ENSP00000495220.2:p.=
ENST00000645114.2:c.2719-6C>T ENSP00000495884.2:p.=
ENST00000645149.2:c.2719-6C>T ENSP00000495944.2:p.=
ENST00000679486.1:c.2719-6C>T ENSP00000506688.1:p.=
ENST00000679629.1:c.2719-6C>T ENSP00000505589.1:p.=
ENST00000679720.1:c.2719-6C>T ENSP00000505938.1:p.=
ENST00000679910.1:c.2719-6C>T ENSP00000506521.1:p.=
ENST00000680001.1:c.*2228-6C>T ENSP00000506351.1:p.=
ENST00000680120.1:c.2719-6C>T ENSP00000504863.1:p.=
ENST00000680137.1:c.2719-6C>T ENSP00000505294.1:p.=
ENST00000680200.1:c.2719-6C>T ENSP00000506166.1:p.=
ENST00000680313.1:c.2719-6C>T ENSP00000506208.1:p.=
ENST00000680423.1:c.2719-6C>T ENSP00000505483.1:p.=
ENST00000680715.1:c.2719-6C>T ENSP00000505332.1:p.=
ENST00000680808.1:c.2719-6C>T ENSP00000506446.1:p.=
ENST00000680874.1:c.2719-6C>T ENSP00000504911.1:p.=
ENST00000681010.1:c.2719-6C>T ENSP00000505201.1:p.=
ENST00000681066.1:c.2719-6C>T ENSP00000506344.1:p.=
ENST00000681123.1:c.2719-6C>T ENSP00000506124.1:p.=
ENST00000681283.1:c.2719-6C>T ENSP00000505667.1:p.=
ENST00000681311.1:c.2719-6C>T ENSP00000505519.1:p.=
ENST00000681321.1:n.982C>T
ENST00000681536.1:c.2719-6C>T ENSP00000505821.1:p.=
ENST00000681574.1:c.2719-6C>T ENSP00000505523.1:p.=
ENST00000681668.1:c.2719-6C>T ENSP00000506420.1:p.=
ENST00000681751.1:c.*2450-6C>T ENSP00000506637.1:p.=
ENST00000681822.1:c.2719-6C>T ENSP00000505744.1:p.=
ENST00000681859.1:c.2719-6C>T ENSP00000505467.1:p.=
ENST00000360184.8:c.2719-6C>T ENSP00000348965.4:p.=
NM_001376.4:c.2719-6C>T NP_001367.2:p.=
NM_001376.5:c.2719-6C>T MANE Select NP_001367.2:p.=