Canonical Allele Identifier: CA2159622809

Gene: DYNC1H1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102039509C= , CM000676.2:g.102039509C=	GRCh38
NC_000014.8:g.102505846C= , CM000676.1:g.102505846C=	GRCh37
NC_000014.7:g.101575599C=	NCBI36
NG_008777.1:g.79982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684561.1:c.*3017C=	ENSP00000506816.1:n.*3017C=
ENST00000360184.10:c.11558C= MANE Select	ENSP00000348965.4:p.Thr3853=
ENST00000553701.1:n.347-2740G=
ENST00000556139.2:n.19C=
ENST00000557242.1:n.329-2740G=
ENST00000557551.1:n.112-2740G=
ENST00000643437.1:n.1512C=
ENST00000643829.1:n.1387C=
ENST00000644794.1:n.1677C=
ENST00000644881.2:c.11558C=	ENSP00000495022.2:p.Thr3853=
ENST00000645039.2:c.11558C=	ENSP00000495220.2:p.Thr3853=
ENST00000645149.2:c.11411C=	ENSP00000495944.2:p.Thr3804=
ENST00000645697.1:n.2221C=
ENST00000647204.2:n.799C=
ENST00000647366.1:n.5112C=
ENST00000679486.1:c.11558C=	ENSP00000506688.1:p.Thr3853=
ENST00000679629.1:c.11558C=	ENSP00000505589.1:p.Thr3853=
ENST00000679720.1:c.11558C=	ENSP00000505938.1:p.Thr3853=
ENST00000679910.1:c.*2640C=	ENSP00000506521.1:n.*2640C=
ENST00000680120.1:c.11558C=	ENSP00000504863.1:p.Thr3853=
ENST00000680200.1:c.*817C=	ENSP00000506166.1:n.*817C=
ENST00000680313.1:c.11558C=	ENSP00000506208.1:p.Thr3853=
ENST00000680423.1:c.*3289C=	ENSP00000505483.1:n.*3289C=
ENST00000680715.1:c.11558C=	ENSP00000505332.1:p.Thr3853=
ENST00000681010.1:c.11558C=	ENSP00000505201.1:p.Thr3853=
ENST00000681066.1:c.11558C=	ENSP00000506344.1:p.Thr3853=
ENST00000681123.1:c.11558C=	ENSP00000506124.1:p.Thr3853=
ENST00000681283.1:c.*270C=	ENSP00000505667.1:n.*270C=
ENST00000681536.1:c.*4757C=	ENSP00000505821.1:n.*4757C=
ENST00000681574.1:c.11558C=	ENSP00000505523.1:p.Thr3853=
ENST00000681822.1:c.11558C=	ENSP00000505744.1:p.Thr3853=
ENST00000360184.8:c.11558C=	ENSP00000348965.4:p.Thr3853=
ENST00000556139.1:n.19C=
NM_001376.4:c.11558C=	NP_001367.2:p.Thr3853=
NM_001376.5:c.11558C= MANE Select	NP_001367.2:p.Thr3853=