Canonical Allele Identifier: CA2038910760
Gene: KIF5A HGNC NCBI

Linked Data

dbSNP Id: rs1882619787

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57581987del , CM000674.2:g.57581987del GRCh38
NC_000012.11:g.57975770del , CM000674.1:g.57975770del GRCh37
NC_000012.10:g.56262037del NCBI36
NG_008155.1:g.36924del

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.2992+35del MANE Select ENSP00000408979.2:n.2992+35del
ENST00000674619.1:c.3013+35del ENSP00000502270.1:n.3013+35del
ENST00000675697.1:c.83+35del
ENST00000675737.1:n.431del
ENST00000675882.1:n.2515+35del
ENST00000675929.1:n.1550+35del
ENST00000676055.1:c.83+35del
ENST00000676437.1:c.17+35del
ENST00000676457.1:c.2887+35del ENSP00000501588.1:n.2887+35del
ENST00000286452.5:c.2725+35del ENSP00000286452.5:n.2725+35del
ENST00000455537.6:c.2992+35del ENSP00000408979.2:n.2992+35del
ENST00000552227.1:n.275+35del
NM_004984.2:c.2992+35del NP_004975.2:n.2992+35del
NM_001354705.1:c.2725+35del NP_001341634.1:n.2725+35del
NM_004984.3:c.2992+35del NP_004975.2:n.2992+35del
XR_002957324.1:n.3225+35del
NM_004984.4:c.2992+35del MANE Select NP_004975.2:n.2992+35del
NM_001354705.2:c.2725+35del NP_001341634.1:n.2725+35del