Canonical Allele Identifier: CA2038935080
Gene: KIF5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57574901T= , CM000674.2:g.57574901T= GRCh38
NC_000012.11:g.57968684T= , CM000674.1:g.57968684T= GRCh37
NC_000012.10:g.56254951T= NCBI36
NG_008155.1:g.29838T=

Transcript Alleles

HGVS Amino-acid change
ENST00000455537.7:c.1717-183T= MANE Select ENSP00000408979.2:n.1717-183T=
ENST00000674619.1:c.1717-183T= ENSP00000502270.1:n.1717-183T=
ENST00000675629.1:c.46-183T= ENSP00000502531.1:n.46-183T=
ENST00000675882.1:n.704-183T=
ENST00000675929.1:n.275-183T=
ENST00000675984.1:n.959-183T=
ENST00000676081.1:n.863-183T=
ENST00000676352.1:c.208-183T= ENSP00000501978.1:n.208-183T=
ENST00000676457.1:c.1612-183T= ENSP00000501588.1:n.1612-183T=
ENST00000286452.5:c.1450-183T= ENSP00000286452.5:n.1450-183T=
ENST00000455537.6:c.1717-183T= ENSP00000408979.2:n.1717-183T=
NM_004984.2:c.1717-183T= NP_004975.2:n.1717-183T=
NM_001354705.1:c.1450-183T= NP_001341634.1:n.1450-183T=
NM_004984.3:c.1717-183T= NP_004975.2:n.1717-183T=
XR_002957324.1:n.1950-183T=
NM_004984.4:c.1717-183T= MANE Select NP_004975.2:n.1717-183T=
NM_001354705.2:c.1450-183T= NP_001341634.1:n.1450-183T=