Canonical Allele Identifier: CA2159623091

Gene: DYNC1H1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102039688C= , CM000676.2:g.102039688C=	GRCh38
NC_000014.8:g.102506025C= , CM000676.1:g.102506025C=	GRCh37
NC_000014.7:g.101575778C=	NCBI36
NG_008777.1:g.80161C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684561.1:c.*3105C=	ENSP00000506816.1:n.*3105C=
ENST00000360184.10:c.11646C= MANE Select	ENSP00000348965.4:p.Thr3882=
ENST00000553701.1:n.347-2919G=
ENST00000556139.2:n.198C=
ENST00000557242.1:n.329-2919G=
ENST00000557551.1:n.112-2919G=
ENST00000643437.1:n.1600C=
ENST00000643829.1:n.1475C=
ENST00000644794.1:n.1765C=
ENST00000644881.2:c.11646C=	ENSP00000495022.2:p.Thr3882=
ENST00000645039.2:c.11646C=	ENSP00000495220.2:p.Thr3882=
ENST00000645085.1:n.143C=
ENST00000645149.2:c.11499C=	ENSP00000495944.2:p.Thr3833=
ENST00000645697.1:n.2309C=
ENST00000647204.2:n.887C=
ENST00000647366.1:n.5200C=
ENST00000679486.1:c.11646C=	ENSP00000506688.1:p.Thr3882=
ENST00000679629.1:c.11646C=	ENSP00000505589.1:p.Thr3882=
ENST00000679720.1:c.11646C=	ENSP00000505938.1:p.Thr3882=
ENST00000679910.1:c.*2728C=	ENSP00000506521.1:n.*2728C=
ENST00000680120.1:c.11646C=	ENSP00000504863.1:p.Thr3882=
ENST00000680200.1:c.*905C=	ENSP00000506166.1:n.*905C=
ENST00000680313.1:c.11646C=	ENSP00000506208.1:p.Thr3882=
ENST00000680423.1:c.*3377C=	ENSP00000505483.1:n.*3377C=
ENST00000680715.1:c.11646C=	ENSP00000505332.1:p.Thr3882=
ENST00000681010.1:c.11646C=	ENSP00000505201.1:p.Thr3882=
ENST00000681066.1:c.11646C=	ENSP00000506344.1:p.Thr3882=
ENST00000681123.1:c.11646C=	ENSP00000506124.1:p.Thr3882=
ENST00000681283.1:c.*358C=	ENSP00000505667.1:n.*358C=
ENST00000681536.1:c.*4845C=	ENSP00000505821.1:n.*4845C=
ENST00000681574.1:c.11646C=	ENSP00000505523.1:p.Thr3882=
ENST00000681822.1:c.11646C=	ENSP00000505744.1:p.Thr3882=
ENST00000360184.8:c.11646C=	ENSP00000348965.4:p.Thr3882=
ENST00000556139.1:n.198C=
NM_001376.4:c.11646C=	NP_001367.2:p.Thr3882=
NM_001376.5:c.11646C= MANE Select	NP_001367.2:p.Thr3882=