Canonical Allele Identifier: CA2159622992

Gene: DYNC1H1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102039606_102039607delinsTG , CM000676.2:g.102039606_102039607delinsTG	GRCh38
NC_000014.8:g.102505943_102505944delinsTG , CM000676.1:g.102505943_102505944delinsTG	GRCh37
NC_000014.7:g.101575696_101575697delinsTG	NCBI36
NG_008777.1:g.80079_80080delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684561.1:c.*3055-32_*3055-31delinsTG	ENSP00000506816.1:n.*3055-32_*3055-31delinsTG
ENST00000360184.10:c.11596-32_11596-31delinsTG MANE Select	ENSP00000348965.4:n.11596-32_11596-31delinsTG
ENST00000553701.1:n.347-2838_347-2837delinsCA
ENST00000556139.2:n.116_117delinsTG
ENST00000557242.1:n.329-2838_329-2837delinsCA
ENST00000557551.1:n.112-2838_112-2837delinsCA
ENST00000643437.1:n.1550-32_1550-31delinsTG
ENST00000643829.1:n.1425-32_1425-31delinsTG
ENST00000644794.1:n.1715-32_1715-31delinsTG
ENST00000644881.2:c.11596-32_11596-31delinsTG	ENSP00000495022.2:n.11596-32_11596-31delinsTG
ENST00000645039.2:c.11596-32_11596-31delinsTG	ENSP00000495220.2:n.11596-32_11596-31delinsTG
ENST00000645085.1:n.61_62delinsTG
ENST00000645149.2:c.11449-32_11449-31delinsTG	ENSP00000495944.2:n.11449-32_11449-31delinsTG
ENST00000645697.1:n.2259-32_2259-31delinsTG
ENST00000647204.2:n.837-32_837-31delinsTG
ENST00000647366.1:n.5150-32_5150-31delinsTG
ENST00000679486.1:c.11596-32_11596-31delinsTG	ENSP00000506688.1:n.11596-32_11596-31delinsTG
ENST00000679629.1:c.11596-32_11596-31delinsTG	ENSP00000505589.1:n.11596-32_11596-31delinsTG
ENST00000679720.1:c.11596-32_11596-31delinsTG	ENSP00000505938.1:n.11596-32_11596-31delinsTG
ENST00000679910.1:c.*2678-32_*2678-31delinsTG	ENSP00000506521.1:n.*2678-32_*2678-31delinsTG
ENST00000680120.1:c.11596-32_11596-31delinsTG	ENSP00000504863.1:n.11596-32_11596-31delinsTG
ENST00000680200.1:c.*855-32_*855-31delinsTG	ENSP00000506166.1:n.*855-32_*855-31delinsTG
ENST00000680313.1:c.11596-32_11596-31delinsTG	ENSP00000506208.1:n.11596-32_11596-31delinsTG
ENST00000680423.1:c.*3327-32_*3327-31delinsTG	ENSP00000505483.1:n.*3327-32_*3327-31delinsTG
ENST00000680715.1:c.11596-32_11596-31delinsTG	ENSP00000505332.1:n.11596-32_11596-31delinsTG
ENST00000681010.1:c.11596-32_11596-31delinsTG	ENSP00000505201.1:n.11596-32_11596-31delinsTG
ENST00000681066.1:c.11596-32_11596-31delinsTG	ENSP00000506344.1:n.11596-32_11596-31delinsTG
ENST00000681123.1:c.11596-32_11596-31delinsTG	ENSP00000506124.1:n.11596-32_11596-31delinsTG
ENST00000681283.1:c.*308-32_*308-31delinsTG	ENSP00000505667.1:n.*308-32_*308-31delinsTG
ENST00000681536.1:c.*4795-32_*4795-31delinsTG	ENSP00000505821.1:n.*4795-32_*4795-31delinsTG
ENST00000681574.1:c.11596-32_11596-31delinsTG	ENSP00000505523.1:n.11596-32_11596-31delinsTG
ENST00000681822.1:c.11596-32_11596-31delinsTG	ENSP00000505744.1:n.11596-32_11596-31delinsTG
ENST00000360184.8:c.11596-32_11596-31delinsTG	ENSP00000348965.4:n.11596-32_11596-31delinsTG
ENST00000556139.1:n.116_117delinsTG
NM_001376.4:c.11596-32_11596-31delinsTG	NP_001367.2:n.11596-32_11596-31delinsTG
NM_001376.5:c.11596-32_11596-31delinsTG MANE Select	NP_001367.2:n.11596-32_11596-31delinsTG