Canonical Allele Identifier: CA385516526

Gene: KIF5A

Linked Data

• MyVariant Identifiers: chr12:g.57975651A>G (hg19) ; chr12:g.57581868A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57581868A>G , CM000674.2:g.57581868A>G	GRCh38
NC_000012.11:g.57975651A>G , CM000674.1:g.57975651A>G	GRCh37
NC_000012.10:g.56261918A>G	NCBI36
NG_008155.1:g.36805A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.2910-2A>G MANE Select	ENSP00000408979.2:n.2910-2A>G
ENST00000674619.1:c.2931-2A>G	ENSP00000502270.1:n.2931-2A>G
ENST00000675737.1:n.314-2A>G
ENST00000675882.1:n.2431A>G
ENST00000675929.1:n.1468-2A>G
ENST00000676457.1:c.2805-2A>G	ENSP00000501588.1:n.2805-2A>G
ENST00000286452.5:c.2643-2A>G	ENSP00000286452.5:n.2643-2A>G
ENST00000455537.6:c.2910-2A>G	ENSP00000408979.2:n.2910-2A>G
ENST00000552227.1:n.191A>G
NM_004984.2:c.2910-2A>G	NP_004975.2:n.2910-2A>G
NM_001354705.1:c.2643-2A>G	NP_001341634.1:n.2643-2A>G
NM_004984.3:c.2910-2A>G	NP_004975.2:n.2910-2A>G
XR_002957324.1:n.3143-2A>G
NM_004984.4:c.2910-2A>G MANE Select	NP_004975.2:n.2910-2A>G
NM_001354705.2:c.2643-2A>G	NP_001341634.1:n.2643-2A>G