Canonical Allele Identifier: CA2038934957
Gene: KIF5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57574808C= , CM000674.2:g.57574808C= GRCh38
NC_000012.11:g.57968591C= , CM000674.1:g.57968591C= GRCh37
NC_000012.10:g.56254858C= NCBI36
NG_008155.1:g.29745C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.1717-276C= MANE Select ENSP00000408979.2:n.1717-276C=
ENST00000674619.1:c.1717-276C= ENSP00000502270.1:n.1717-276C=
ENST00000675629.1:c.46-276C= ENSP00000502531.1:n.46-276C=
ENST00000675882.1:n.704-276C=
ENST00000675929.1:n.275-276C=
ENST00000675984.1:n.959-276C=
ENST00000676081.1:n.863-276C=
ENST00000676352.1:c.208-276C= ENSP00000501978.1:n.208-276C=
ENST00000676457.1:c.1612-276C= ENSP00000501588.1:n.1612-276C=
ENST00000286452.5:c.1450-276C= ENSP00000286452.5:n.1450-276C=
ENST00000455537.6:c.1717-276C= ENSP00000408979.2:n.1717-276C=
NM_004984.2:c.1717-276C= NP_004975.2:n.1717-276C=
NM_001354705.1:c.1450-276C= NP_001341634.1:n.1450-276C=
NM_004984.3:c.1717-276C= NP_004975.2:n.1717-276C=
XR_002957324.1:n.1950-276C=
NM_004984.4:c.1717-276C= MANE Select NP_004975.2:n.1717-276C=
NM_001354705.2:c.1450-276C= NP_001341634.1:n.1450-276C=