Canonical Allele Identifier: CA391034989

Gene: DYNC1H1

Linked Data

• dbSNP Id: rs1262187792
• MyVariant Identifiers: chr14:g.102506005C>G (hg19) ; chr14:g.102039668C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102039668C>G , CM000676.2:g.102039668C>G	GRCh38
NC_000014.8:g.102506005C>G , CM000676.1:g.102506005C>G	GRCh37
NC_000014.7:g.101575758C>G	NCBI36
NG_008777.1:g.80141C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684561.1:c.*3085C>G	ENSP00000506816.1:n.*3085C>G
ENST00000360184.10:c.11626C>G MANE Select	ENSP00000348965.4:p.Leu3876Val
ENST00000553701.1:n.347-2899G>C
ENST00000556139.2:n.178C>G
ENST00000557242.1:n.329-2899G>C
ENST00000557551.1:n.112-2899G>C
ENST00000643437.1:n.1580C>G
ENST00000643829.1:n.1455C>G
ENST00000644794.1:n.1745C>G
ENST00000644881.2:c.11626C>G	ENSP00000495022.2:p.Leu3876Val
ENST00000645039.2:c.11626C>G	ENSP00000495220.2:p.Leu3876Val
ENST00000645085.1:n.123C>G
ENST00000645149.2:c.11479C>G	ENSP00000495944.2:p.Leu3827Val
ENST00000645697.1:n.2289C>G
ENST00000647204.2:n.867C>G
ENST00000647366.1:n.5180C>G
ENST00000679486.1:c.11626C>G	ENSP00000506688.1:p.Leu3876Val
ENST00000679629.1:c.11626C>G	ENSP00000505589.1:p.Leu3876Val
ENST00000679720.1:c.11626C>G	ENSP00000505938.1:p.Leu3876Val
ENST00000679910.1:c.*2708C>G	ENSP00000506521.1:n.*2708C>G
ENST00000680120.1:c.11626C>G	ENSP00000504863.1:p.Leu3876Val
ENST00000680200.1:c.*885C>G	ENSP00000506166.1:n.*885C>G
ENST00000680313.1:c.11626C>G	ENSP00000506208.1:p.Leu3876Val
ENST00000680423.1:c.*3357C>G	ENSP00000505483.1:n.*3357C>G
ENST00000680715.1:c.11626C>G	ENSP00000505332.1:p.Leu3876Val
ENST00000681010.1:c.11626C>G	ENSP00000505201.1:p.Leu3876Val
ENST00000681066.1:c.11626C>G	ENSP00000506344.1:p.Leu3876Val
ENST00000681123.1:c.11626C>G	ENSP00000506124.1:p.Leu3876Val
ENST00000681283.1:c.*338C>G	ENSP00000505667.1:n.*338C>G
ENST00000681536.1:c.*4825C>G	ENSP00000505821.1:n.*4825C>G
ENST00000681574.1:c.11626C>G	ENSP00000505523.1:p.Leu3876Val
ENST00000681822.1:c.11626C>G	ENSP00000505744.1:p.Leu3876Val
ENST00000360184.8:c.11626C>G	ENSP00000348965.4:p.Leu3876Val
ENST00000556139.1:n.178C>G
NM_001376.4:c.11626C>G	NP_001367.2:p.Leu3876Val
NM_001376.5:c.11626C>G MANE Select	NP_001367.2:p.Leu3876Val