Canonical Allele Identifier: CA385516555

Gene: KIF5A

Linked Data

• MyVariant Identifiers: chr12:g.57975664C>A (hg19) ; chr12:g.57581881C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57581881C>A , CM000674.2:g.57581881C>A	GRCh38
NC_000012.11:g.57975664C>A , CM000674.1:g.57975664C>A	GRCh37
NC_000012.10:g.56261931C>A	NCBI36
NG_008155.1:g.36818C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.2921C>A MANE Select	ENSP00000408979.2:p.Ser974Tyr
ENST00000674619.1:c.2942C>A	ENSP00000502270.1:p.Ser981Tyr
ENST00000675697.1:c.12C>A
ENST00000675737.1:n.325C>A
ENST00000675882.1:n.2444C>A
ENST00000675929.1:n.1479C>A
ENST00000676055.1:c.12C>A
ENST00000676457.1:c.2816C>A	ENSP00000501588.1:p.Ser939Tyr
ENST00000286452.5:c.2654C>A	ENSP00000286452.5:p.Ser885Tyr
ENST00000455537.6:c.2921C>A	ENSP00000408979.2:p.Ser974Tyr
ENST00000552227.1:n.204C>A
NM_004984.2:c.2921C>A	NP_004975.2:p.Ser974Tyr
NM_001354705.1:c.2654C>A	NP_001341634.1:p.Ser885Tyr
NM_004984.3:c.2921C>A	NP_004975.2:p.Ser974Tyr
XR_002957324.1:n.3154C>A
NM_004984.4:c.2921C>A MANE Select	NP_004975.2:p.Ser974Tyr
NM_001354705.2:c.2654C>A	NP_001341634.1:p.Ser885Tyr