Canonical Allele Identifier: CA2619476745
Gene: KIF5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57574949A>G , CM000674.2:g.57574949A>G GRCh38
NC_000012.11:g.57968732A>G , CM000674.1:g.57968732A>G GRCh37
NC_000012.10:g.56254999A>G NCBI36
NG_008155.1:g.29886A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000455537.7:c.1717-135A>G MANE Select ENSP00000408979.2:n.1717-135A>G
ENST00000674619.1:c.1717-135A>G ENSP00000502270.1:n.1717-135A>G
ENST00000675629.1:c.46-135A>G ENSP00000502531.1:n.46-135A>G
ENST00000675882.1:n.704-135A>G
ENST00000675929.1:n.275-135A>G
ENST00000675984.1:n.959-135A>G
ENST00000676081.1:n.863-135A>G
ENST00000676352.1:c.208-135A>G ENSP00000501978.1:n.208-135A>G
ENST00000676457.1:c.1612-135A>G ENSP00000501588.1:n.1612-135A>G
ENST00000286452.5:c.1450-135A>G ENSP00000286452.5:n.1450-135A>G
ENST00000455537.6:c.1717-135A>G ENSP00000408979.2:n.1717-135A>G
NM_004984.2:c.1717-135A>G NP_004975.2:n.1717-135A>G
NM_001354705.1:c.1450-135A>G NP_001341634.1:n.1450-135A>G
NM_004984.3:c.1717-135A>G NP_004975.2:n.1717-135A>G
XR_002957324.1:n.1950-135A>G
NM_004984.4:c.1717-135A>G MANE Select NP_004975.2:n.1717-135A>G
NM_001354705.2:c.1450-135A>G NP_001341634.1:n.1450-135A>G