Canonical Allele Identifier: CA2038910969

Gene: KIF5A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57582100C= , CM000674.2:g.57582100C=	GRCh38
NC_000012.11:g.57975883C= , CM000674.1:g.57975883C=	GRCh37
NC_000012.10:g.56262150C=	NCBI36
NG_008155.1:g.37037C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.2992+148C= MANE Select	ENSP00000408979.2:n.2992+148C=
ENST00000674619.1:c.3013+148C=	ENSP00000502270.1:n.3013+148C=
ENST00000675697.1:c.83+148C=
ENST00000675737.1:n.544C=
ENST00000675882.1:n.2515+148C=
ENST00000675929.1:n.1550+148C=
ENST00000676055.1:c.83+148C=
ENST00000676437.1:c.17+148C=
ENST00000676457.1:c.2887+148C=	ENSP00000501588.1:n.2887+148C=
ENST00000286452.5:c.2725+148C=	ENSP00000286452.5:n.2725+148C=
ENST00000455537.6:c.2992+148C=	ENSP00000408979.2:n.2992+148C=
ENST00000552227.1:n.275+148C=
NM_004984.2:c.2992+148C=	NP_004975.2:n.2992+148C=
NM_001354705.1:c.2725+148C=	NP_001341634.1:n.2725+148C=
NM_004984.3:c.2992+148C=	NP_004975.2:n.2992+148C=
XR_002957324.1:n.3225+148C=
NM_004984.4:c.2992+148C= MANE Select	NP_004975.2:n.2992+148C=
NM_001354705.2:c.2725+148C=	NP_001341634.1:n.2725+148C=