Canonical Allele Identifier: CA2619476692
Gene: KIF5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57574945G>A , CM000674.2:g.57574945G>A GRCh38
NC_000012.11:g.57968728G>A , CM000674.1:g.57968728G>A GRCh37
NC_000012.10:g.56254995G>A NCBI36
NG_008155.1:g.29882G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000455537.7:c.1717-139G>A MANE Select ENSP00000408979.2:n.1717-139G>A
ENST00000674619.1:c.1717-139G>A ENSP00000502270.1:n.1717-139G>A
ENST00000675629.1:c.46-139G>A ENSP00000502531.1:n.46-139G>A
ENST00000675882.1:n.704-139G>A
ENST00000675929.1:n.275-139G>A
ENST00000675984.1:n.959-139G>A
ENST00000676081.1:n.863-139G>A
ENST00000676352.1:c.208-139G>A ENSP00000501978.1:n.208-139G>A
ENST00000676457.1:c.1612-139G>A ENSP00000501588.1:n.1612-139G>A
ENST00000286452.5:c.1450-139G>A ENSP00000286452.5:n.1450-139G>A
ENST00000455537.6:c.1717-139G>A ENSP00000408979.2:n.1717-139G>A
NM_004984.2:c.1717-139G>A NP_004975.2:n.1717-139G>A
NM_001354705.1:c.1450-139G>A NP_001341634.1:n.1450-139G>A
NM_004984.3:c.1717-139G>A NP_004975.2:n.1717-139G>A
XR_002957324.1:n.1950-139G>A
NM_004984.4:c.1717-139G>A MANE Select NP_004975.2:n.1717-139G>A
NM_001354705.2:c.1450-139G>A NP_001341634.1:n.1450-139G>A