Canonical Allele Identifier: CA2038935153

Gene: KIF5A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57574954C= , CM000674.2:g.57574954C=	GRCh38
NC_000012.11:g.57968737C= , CM000674.1:g.57968737C=	GRCh37
NC_000012.10:g.56255004C=	NCBI36
NG_008155.1:g.29891C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.1717-130C= MANE Select	ENSP00000408979.2:n.1717-130C=
ENST00000674619.1:c.1717-130C=	ENSP00000502270.1:n.1717-130C=
ENST00000675629.1:c.46-130C=	ENSP00000502531.1:n.46-130C=
ENST00000675882.1:n.704-130C=
ENST00000675929.1:n.275-130C=
ENST00000675984.1:n.959-130C=
ENST00000676081.1:n.863-130C=
ENST00000676352.1:c.208-130C=	ENSP00000501978.1:n.208-130C=
ENST00000676457.1:c.1612-130C=	ENSP00000501588.1:n.1612-130C=
ENST00000286452.5:c.1450-130C=	ENSP00000286452.5:n.1450-130C=
ENST00000455537.6:c.1717-130C=	ENSP00000408979.2:n.1717-130C=
NM_004984.2:c.1717-130C=	NP_004975.2:n.1717-130C=
NM_001354705.1:c.1450-130C=	NP_001341634.1:n.1450-130C=
NM_004984.3:c.1717-130C=	NP_004975.2:n.1717-130C=
XR_002957324.1:n.1950-130C=
NM_004984.4:c.1717-130C= MANE Select	NP_004975.2:n.1717-130C=
NM_001354705.2:c.1450-130C=	NP_001341634.1:n.1450-130C=