Canonical Allele Identifier: CA385516538

Gene: KIF5A

Linked Data

• MyVariant Identifiers: chr12:g.57975656T>A (hg19) ; chr12:g.57581873T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57581873T>A , CM000674.2:g.57581873T>A	GRCh38
NC_000012.11:g.57975656T>A , CM000674.1:g.57975656T>A	GRCh37
NC_000012.10:g.56261923T>A	NCBI36
NG_008155.1:g.36810T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.2913T>A MANE Select	ENSP00000408979.2:p.Phe971Leu
ENST00000674619.1:c.2934T>A	ENSP00000502270.1:p.Phe978Leu
ENST00000675697.1:c.4T>A
ENST00000675737.1:n.317T>A
ENST00000675882.1:n.2436T>A
ENST00000675929.1:n.1471T>A
ENST00000676055.1:c.4T>A
ENST00000676457.1:c.2808T>A	ENSP00000501588.1:p.Phe936Leu
ENST00000286452.5:c.2646T>A	ENSP00000286452.5:p.Phe882Leu
ENST00000455537.6:c.2913T>A	ENSP00000408979.2:p.Phe971Leu
ENST00000552227.1:n.196T>A
NM_004984.2:c.2913T>A	NP_004975.2:p.Phe971Leu
NM_001354705.1:c.2646T>A	NP_001341634.1:p.Phe882Leu
NM_004984.3:c.2913T>A	NP_004975.2:p.Phe971Leu
XR_002957324.1:n.3146T>A
NM_004984.4:c.2913T>A MANE Select	NP_004975.2:p.Phe971Leu
NM_001354705.2:c.2646T>A	NP_001341634.1:p.Phe882Leu