Canonical Allele Identifier: CA2159591920

Gene: DYNC1H1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.101982978A= , CM000676.2:g.101982978A=	GRCh38
NC_000014.8:g.102449315A= , CM000676.1:g.102449315A=	GRCh37
NC_000014.7:g.101519068A=	NCBI36
NG_008777.1:g.23451A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684561.1:c.962-41A=	ENSP00000506816.1:n.962-41A=
ENST00000360184.10:c.962-41A= MANE Select	ENSP00000348965.4:n.962-41A=
ENST00000643508.2:c.962-41A=	ENSP00000495528.2:n.962-41A=
ENST00000643684.1:n.1081-41A=
ENST00000643958.2:c.962-41A=	ENSP00000505734.1:n.962-41A=
ENST00000644881.2:c.962-41A=	ENSP00000495022.2:n.962-41A=
ENST00000645039.2:c.962-41A=	ENSP00000495220.2:n.962-41A=
ENST00000645114.2:c.962-41A=	ENSP00000495884.2:n.962-41A=
ENST00000645149.2:c.962-41A=	ENSP00000495944.2:n.962-41A=
ENST00000679486.1:c.962-41A=	ENSP00000506688.1:n.962-41A=
ENST00000679629.1:c.962-41A=	ENSP00000505589.1:n.962-41A=
ENST00000679720.1:c.962-41A=	ENSP00000505938.1:n.962-41A=
ENST00000679910.1:c.962-41A=	ENSP00000506521.1:n.962-41A=
ENST00000680001.1:c.*471-41A=	ENSP00000506351.1:n.*471-41A=
ENST00000680120.1:c.962-41A=	ENSP00000504863.1:n.962-41A=
ENST00000680137.1:c.962-41A=	ENSP00000505294.1:n.962-41A=
ENST00000680200.1:c.962-41A=	ENSP00000506166.1:n.962-41A=
ENST00000680313.1:c.962-41A=	ENSP00000506208.1:n.962-41A=
ENST00000680423.1:c.962-41A=	ENSP00000505483.1:n.962-41A=
ENST00000680715.1:c.962-41A=	ENSP00000505332.1:n.962-41A=
ENST00000680808.1:c.962-41A=	ENSP00000506446.1:n.962-41A=
ENST00000680874.1:c.962-41A=	ENSP00000504911.1:n.962-41A=
ENST00000681010.1:c.962-41A=	ENSP00000505201.1:n.962-41A=
ENST00000681066.1:c.962-41A=	ENSP00000506344.1:n.962-41A=
ENST00000681123.1:c.962-41A=	ENSP00000506124.1:n.962-41A=
ENST00000681283.1:c.962-41A=	ENSP00000505667.1:n.962-41A=
ENST00000681311.1:c.962-41A=	ENSP00000505519.1:n.962-41A=
ENST00000681536.1:c.962-41A=	ENSP00000505821.1:n.962-41A=
ENST00000681574.1:c.962-41A=	ENSP00000505523.1:n.962-41A=
ENST00000681668.1:c.962-41A=	ENSP00000506420.1:n.962-41A=
ENST00000681751.1:c.*693-41A=	ENSP00000506637.1:n.*693-41A=
ENST00000681822.1:c.962-41A=	ENSP00000505744.1:n.962-41A=
ENST00000681859.1:c.962-41A=	ENSP00000505467.1:n.962-41A=
ENST00000360184.8:c.962-41A=	ENSP00000348965.4:n.962-41A=
NM_001376.4:c.962-41A=	NP_001367.2:n.962-41A=
NM_001376.5:c.962-41A= MANE Select	NP_001367.2:n.962-41A=