Canonical Allele Identifier: CA2573148855
Gene: KIF5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1575200
ClinVar RCV Id: RCV002073794
dbSNP Id: rs2140162529

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57568952T>G , CM000674.2:g.57568952T>G GRCh38
NC_000012.11:g.57962735T>G , CM000674.1:g.57962735T>G GRCh37
NC_000012.10:g.56249002T>G NCBI36
NG_008155.1:g.23889T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.715-11T>G MANE Select ENSP00000408979.2:n.715-11T>G
ENST00000674619.1:c.715-11T>G ENSP00000502270.1:n.715-11T>G
ENST00000676457.1:c.610-11T>G ENSP00000501588.1:n.610-11T>G
ENST00000286452.5:c.448-11T>G ENSP00000286452.5:n.448-11T>G
ENST00000455537.6:c.715-11T>G ENSP00000408979.2:n.715-11T>G
NM_004984.2:c.715-11T>G NP_004975.2:n.715-11T>G
NM_001354705.1:c.448-11T>G NP_001341634.1:n.448-11T>G
NM_004984.3:c.715-11T>G NP_004975.2:n.715-11T>G
XR_002957324.1:n.948-11T>G
NM_004984.4:c.715-11T>G MANE Select NP_004975.2:n.715-11T>G
NM_001354705.2:c.448-11T>G NP_001341634.1:n.448-11T>G