Canonical Allele Identifier: CA6653066

Gene: KIF5A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57576852C>A , CM000674.2:g.57576852C>A	GRCh38
NC_000012.11:g.57970635C>A , CM000674.1:g.57970635C>A	GRCh37
NC_000012.10:g.56256902C>A	NCBI36
NG_008155.1:g.31789C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004984.4:c.2290C>A MANE Select	NP_004975.2:p.Gln764Lys
ENST00000455537.7:c.2290C>A MANE Select	ENSP00000408979.2:p.Gln764Lys
NM_001354705.1:c.2023C>A	NP_001341634.1:p.Gln675Lys
NM_001354705.2:c.2023C>A	NP_001341634.1:p.Gln675Lys
NM_004984.2:c.2290C>A	NP_004975.2:p.Gln764Lys
NM_004984.3:c.2290C>A	NP_004975.2:p.Gln764Lys
ENST00000286452.5:c.2023C>A	ENSP00000286452.5:p.Gln675Lys
ENST00000455537.6:c.2290C>A	ENSP00000408979.2:p.Gln764Lys
ENST00000674619.1:c.2290C>A	ENSP00000502270.1:p.Gln764Lys
ENST00000675299.1:c.438C>A	ENSP00000501888.1:n.438C>A
ENST00000675397.1:n.60C>A
ENST00000675882.1:n.1277C>A
ENST00000675929.1:n.848C>A
ENST00000675984.1:n.2360C>A
ENST00000676081.1:n.1935C>A
ENST00000676457.1:c.2185C>A	ENSP00000501588.1:p.Gln729Lys
XR_002957324.1:n.2523C>A