Canonical Allele Identifier: CA2159623052

Gene: DYNC1H1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102039642C= , CM000676.2:g.102039642C=	GRCh38
NC_000014.8:g.102505979C= , CM000676.1:g.102505979C=	GRCh37
NC_000014.7:g.101575732C=	NCBI36
NG_008777.1:g.80115C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684561.1:c.*3059C=	ENSP00000506816.1:n.*3059C=
ENST00000360184.10:c.11600C= MANE Select	ENSP00000348965.4:p.Ala3867=
ENST00000553701.1:n.347-2873G=
ENST00000556139.2:n.152C=
ENST00000557242.1:n.329-2873G=
ENST00000557551.1:n.112-2873G=
ENST00000643437.1:n.1554C=
ENST00000643829.1:n.1429C=
ENST00000644794.1:n.1719C=
ENST00000644881.2:c.11600C=	ENSP00000495022.2:p.Ala3867=
ENST00000645039.2:c.11600C=	ENSP00000495220.2:p.Ala3867=
ENST00000645085.1:n.97C=
ENST00000645149.2:c.11453C=	ENSP00000495944.2:p.Ala3818=
ENST00000645697.1:n.2263C=
ENST00000647204.2:n.841C=
ENST00000647366.1:n.5154C=
ENST00000679486.1:c.11600C=	ENSP00000506688.1:p.Ala3867=
ENST00000679629.1:c.11600C=	ENSP00000505589.1:p.Ala3867=
ENST00000679720.1:c.11600C=	ENSP00000505938.1:p.Ala3867=
ENST00000679910.1:c.*2682C=	ENSP00000506521.1:n.*2682C=
ENST00000680120.1:c.11600C=	ENSP00000504863.1:p.Ala3867=
ENST00000680200.1:c.*859C=	ENSP00000506166.1:n.*859C=
ENST00000680313.1:c.11600C=	ENSP00000506208.1:p.Ala3867=
ENST00000680423.1:c.*3331C=	ENSP00000505483.1:n.*3331C=
ENST00000680715.1:c.11600C=	ENSP00000505332.1:p.Ala3867=
ENST00000681010.1:c.11600C=	ENSP00000505201.1:p.Ala3867=
ENST00000681066.1:c.11600C=	ENSP00000506344.1:p.Ala3867=
ENST00000681123.1:c.11600C=	ENSP00000506124.1:p.Ala3867=
ENST00000681283.1:c.*312C=	ENSP00000505667.1:n.*312C=
ENST00000681536.1:c.*4799C=	ENSP00000505821.1:n.*4799C=
ENST00000681574.1:c.11600C=	ENSP00000505523.1:p.Ala3867=
ENST00000681822.1:c.11600C=	ENSP00000505744.1:p.Ala3867=
ENST00000360184.8:c.11600C=	ENSP00000348965.4:p.Ala3867=
ENST00000556139.1:n.152C=
NM_001376.4:c.11600C=	NP_001367.2:p.Ala3867=
NM_001376.5:c.11600C= MANE Select	NP_001367.2:p.Ala3867=