Canonical Allele Identifier: CA480264122
Gene: KIF5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2018127
ClinVar RCV Id: RCV002861842
dbSNP Id: rs1882167842
MyVariant Identifiers: chr12:g.57963044C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57569261C>T , CM000674.2:g.57569261C>T GRCh38
NC_000012.11:g.57963044C>T , CM000674.1:g.57963044C>T GRCh37
NC_000012.10:g.56249311C>T NCBI36
NG_008155.1:g.24198C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.825C>T MANE Select ENSP00000408979.2:p.Ser275=
ENST00000674619.1:c.825C>T ENSP00000502270.1:p.Ser275=
ENST00000676457.1:c.720C>T ENSP00000501588.1:p.Ser240=
ENST00000286452.5:c.558C>T ENSP00000286452.5:p.Ser186=
ENST00000455537.6:c.825C>T ENSP00000408979.2:p.Ser275=
NM_004984.2:c.825C>T NP_004975.2:p.Ser275=
NM_001354705.1:c.558C>T NP_001341634.1:p.Ser186=
NM_004984.3:c.825C>T NP_004975.2:p.Ser275=
XR_002957324.1:n.1058C>T
NM_004984.4:c.825C>T MANE Select NP_004975.2:p.Ser275=
NM_001354705.2:c.558C>T NP_001341634.1:p.Ser186=