Canonical Allele Identifier: CA690303634

Gene: KIF5A

Linked Data

• dbSNP Id: rs1288910093
• MyVariant Identifiers: chr12:g.57963002T>A (hg19) ; chr12:g.57569219T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57569219T>A , CM000674.2:g.57569219T>A	GRCh38
NC_000012.11:g.57963002T>A , CM000674.1:g.57963002T>A	GRCh37
NC_000012.10:g.56249269T>A	NCBI36
NG_008155.1:g.24156T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.820-37T>A MANE Select	ENSP00000408979.2:n.820-37T>A
ENST00000674619.1:c.820-37T>A	ENSP00000502270.1:n.820-37T>A
ENST00000676457.1:c.715-37T>A	ENSP00000501588.1:n.715-37T>A
ENST00000286452.5:c.553-37T>A	ENSP00000286452.5:n.553-37T>A
ENST00000455537.6:c.820-37T>A	ENSP00000408979.2:n.820-37T>A
NM_004984.2:c.820-37T>A	NP_004975.2:n.820-37T>A
NM_001354705.1:c.553-37T>A	NP_001341634.1:n.553-37T>A
NM_004984.3:c.820-37T>A	NP_004975.2:n.820-37T>A
XR_002957324.1:n.1053-37T>A
NM_004984.4:c.820-37T>A MANE Select	NP_004975.2:n.820-37T>A
NM_001354705.2:c.553-37T>A	NP_001341634.1:n.553-37T>A