Canonical Allele Identifier: CA2619476608
Gene: KIF5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57574933T>G , CM000674.2:g.57574933T>G GRCh38
NC_000012.11:g.57968716T>G , CM000674.1:g.57968716T>G GRCh37
NC_000012.10:g.56254983T>G NCBI36
NG_008155.1:g.29870T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000455537.7:c.1717-151T>G MANE Select ENSP00000408979.2:n.1717-151T>G
ENST00000674619.1:c.1717-151T>G ENSP00000502270.1:n.1717-151T>G
ENST00000675629.1:c.46-151T>G ENSP00000502531.1:n.46-151T>G
ENST00000675882.1:n.704-151T>G
ENST00000675929.1:n.275-151T>G
ENST00000675984.1:n.959-151T>G
ENST00000676081.1:n.863-151T>G
ENST00000676352.1:c.208-151T>G ENSP00000501978.1:n.208-151T>G
ENST00000676457.1:c.1612-151T>G ENSP00000501588.1:n.1612-151T>G
ENST00000286452.5:c.1450-151T>G ENSP00000286452.5:n.1450-151T>G
ENST00000455537.6:c.1717-151T>G ENSP00000408979.2:n.1717-151T>G
NM_004984.2:c.1717-151T>G NP_004975.2:n.1717-151T>G
NM_001354705.1:c.1450-151T>G NP_001341634.1:n.1450-151T>G
NM_004984.3:c.1717-151T>G NP_004975.2:n.1717-151T>G
XR_002957324.1:n.1950-151T>G
NM_004984.4:c.1717-151T>G MANE Select NP_004975.2:n.1717-151T>G
NM_001354705.2:c.1450-151T>G NP_001341634.1:n.1450-151T>G