Canonical Allele Identifier: CA2159622438

Gene: DYNC1H1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102039251G= , CM000676.2:g.102039251G=	GRCh38
NC_000014.8:g.102505588G= , CM000676.1:g.102505588G=	GRCh37
NC_000014.7:g.101575341G=	NCBI36
NG_008777.1:g.79724G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684561.1:c.*2916G=	ENSP00000506816.1:n.*2916G=
ENST00000360184.10:c.11457G= MANE Select	ENSP00000348965.4:p.Lys3819=
ENST00000553701.1:n.347-2482C=
ENST00000557242.1:n.329-2482C=
ENST00000557551.1:n.112-2482C=
ENST00000643437.1:n.1411G=
ENST00000643829.1:n.1286G=
ENST00000644794.1:n.1576G=
ENST00000644881.2:c.11457G=	ENSP00000495022.2:p.Lys3819=
ENST00000645039.2:c.11457G=	ENSP00000495220.2:p.Lys3819=
ENST00000645149.2:c.11310G=	ENSP00000495944.2:p.Lys3770=
ENST00000645697.1:n.2120G=
ENST00000647204.2:n.698G=
ENST00000647366.1:n.5011G=
ENST00000679486.1:c.11457G=	ENSP00000506688.1:p.Lys3819=
ENST00000679629.1:c.11457G=	ENSP00000505589.1:p.Lys3819=
ENST00000679720.1:c.11457G=	ENSP00000505938.1:p.Lys3819=
ENST00000679910.1:c.*2539G=	ENSP00000506521.1:n.*2539G=
ENST00000680120.1:c.11457G=	ENSP00000504863.1:p.Lys3819=
ENST00000680200.1:c.*716G=	ENSP00000506166.1:n.*716G=
ENST00000680313.1:c.11457G=	ENSP00000506208.1:p.Lys3819=
ENST00000680423.1:c.*3188G=	ENSP00000505483.1:n.*3188G=
ENST00000680715.1:c.11457G=	ENSP00000505332.1:p.Lys3819=
ENST00000681010.1:c.11457G=	ENSP00000505201.1:p.Lys3819=
ENST00000681066.1:c.11457G=	ENSP00000506344.1:p.Lys3819=
ENST00000681123.1:c.11457G=	ENSP00000506124.1:p.Lys3819=
ENST00000681283.1:c.*169G=	ENSP00000505667.1:n.*169G=
ENST00000681536.1:c.*4656G=	ENSP00000505821.1:n.*4656G=
ENST00000681574.1:c.11457G=	ENSP00000505523.1:p.Lys3819=
ENST00000681822.1:c.11457G=	ENSP00000505744.1:p.Lys3819=
ENST00000360184.8:c.11457G=	ENSP00000348965.4:p.Lys3819=
NM_001376.4:c.11457G=	NP_001367.2:p.Lys3819=
NM_001376.5:c.11457G= MANE Select	NP_001367.2:p.Lys3819=