Canonical Allele Identifier: CA948096626
Gene: KIF5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57582073T>A , CM000674.2:g.57582073T>A GRCh38
NC_000012.11:g.57975856T>A , CM000674.1:g.57975856T>A GRCh37
NC_000012.10:g.56262123T>A NCBI36
NG_008155.1:g.37010T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.2992+121T>A MANE Select ENSP00000408979.2:n.2992+121T>A
ENST00000674619.1:c.3013+121T>A ENSP00000502270.1:n.3013+121T>A
ENST00000675697.1:c.83+121T>A
ENST00000675737.1:n.517T>A
ENST00000675882.1:n.2515+121T>A
ENST00000675929.1:n.1550+121T>A
ENST00000676055.1:c.83+121T>A
ENST00000676437.1:c.17+121T>A
ENST00000676457.1:c.2887+121T>A ENSP00000501588.1:n.2887+121T>A
ENST00000286452.5:c.2725+121T>A ENSP00000286452.5:n.2725+121T>A
ENST00000455537.6:c.2992+121T>A ENSP00000408979.2:n.2992+121T>A
ENST00000552227.1:n.275+121T>A
NM_004984.2:c.2992+121T>A NP_004975.2:n.2992+121T>A
NM_001354705.1:c.2725+121T>A NP_001341634.1:n.2725+121T>A
NM_004984.3:c.2992+121T>A NP_004975.2:n.2992+121T>A
XR_002957324.1:n.3225+121T>A
NM_004984.4:c.2992+121T>A MANE Select NP_004975.2:n.2992+121T>A
NM_001354705.2:c.2725+121T>A NP_001341634.1:n.2725+121T>A