Canonical Allele Identifier: CA480266246
Gene: KIF5A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.57975698C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57581915C>A , CM000674.2:g.57581915C>A GRCh38
NC_000012.11:g.57975698C>A , CM000674.1:g.57975698C>A GRCh37
NC_000012.10:g.56261965C>A NCBI36
NG_008155.1:g.36852C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.2955C>A MANE Select ENSP00000408979.2:p.Gly985=
ENST00000674619.1:c.2976C>A ENSP00000502270.1:p.Gly992=
ENST00000675697.1:c.46C>A
ENST00000675737.1:n.359C>A
ENST00000675882.1:n.2478C>A
ENST00000675929.1:n.1513C>A
ENST00000676055.1:c.46C>A
ENST00000676457.1:c.2850C>A ENSP00000501588.1:p.Gly950=
ENST00000286452.5:c.2688C>A ENSP00000286452.5:p.Gly896=
ENST00000455537.6:c.2955C>A ENSP00000408979.2:p.Gly985=
ENST00000552227.1:n.238C>A
NM_004984.2:c.2955C>A NP_004975.2:p.Gly985=
NM_001354705.1:c.2688C>A NP_001341634.1:p.Gly896=
NM_004984.3:c.2955C>A NP_004975.2:p.Gly985=
XR_002957324.1:n.3188C>A
NM_004984.4:c.2955C>A MANE Select NP_004975.2:p.Gly985=
NM_001354705.2:c.2688C>A NP_001341634.1:p.Gly896=