Canonical Allele Identifier: CA487969423

Gene: DYNC1H1

Linked Data

• MyVariant Identifiers: chr14:g.102514858T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.102048521T>A , CM000676.2:g.102048521T>A	GRCh38
NC_000014.8:g.102514858T>A , CM000676.1:g.102514858T>A	GRCh37
NC_000014.7:g.101584611T>A	NCBI36
NG_008777.1:g.88994T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684561.1:c.*4683T>A	ENSP00000506816.1:n.*4683T>A
ENST00000360184.10:c.13224T>A MANE Select	ENSP00000348965.4:p.Pro4408=
ENST00000553701.1:n.346+1924A>T
ENST00000555062.2:n.297T>A
ENST00000556229.2:n.617T>A
ENST00000557242.1:n.328+4006A>T
ENST00000643437.1:n.3178T>A
ENST00000643591.1:n.1017T>A
ENST00000643729.1:n.857T>A
ENST00000643829.1:n.3180T>A
ENST00000644239.2:n.1360T>A
ENST00000644794.1:n.3830T>A
ENST00000644881.2:c.13224T>A	ENSP00000495022.2:p.Pro4408=
ENST00000645039.2:c.*1075T>A	ENSP00000495220.2:n.*1075T>A
ENST00000645085.1:n.1470T>A
ENST00000645149.2:c.13077T>A	ENSP00000495944.2:p.Pro4359=
ENST00000647143.1:n.859T>A
ENST00000647204.2:n.2560T>A
ENST00000647366.1:n.6778T>A
ENST00000679720.1:c.13224T>A	ENSP00000505938.1:p.Pro4408=
ENST00000679910.1:c.*4306T>A	ENSP00000506521.1:n.*4306T>A
ENST00000680120.1:c.13219-9T>A	ENSP00000504863.1:n.13219-9T>A
ENST00000680178.1:n.783T>A
ENST00000680200.1:c.*2483T>A	ENSP00000506166.1:n.*2483T>A
ENST00000680313.1:c.13224T>A	ENSP00000506208.1:p.Pro4408=
ENST00000680423.1:c.*4955T>A	ENSP00000505483.1:n.*4955T>A
ENST00000680715.1:c.*514T>A	ENSP00000505332.1:n.*514T>A
ENST00000681066.1:c.*1247T>A	ENSP00000506344.1:n.*1247T>A
ENST00000681283.1:c.*1936T>A	ENSP00000505667.1:n.*1936T>A
ENST00000681536.1:c.*6423T>A	ENSP00000505821.1:n.*6423T>A
ENST00000681574.1:c.13224T>A	ENSP00000505523.1:p.Pro4408=
ENST00000681822.1:c.13224T>A	ENSP00000505744.1:p.Pro4408=
ENST00000360184.8:c.13224T>A	ENSP00000348965.4:p.Pro4408=
ENST00000555062.1:n.274T>A
ENST00000556229.1:n.374T>A
NM_001376.4:c.13224T>A	NP_001367.2:p.Pro4408=
NM_001376.5:c.13224T>A MANE Select	NP_001367.2:p.Pro4408=