Canonical Allele Identifier: CA480266213

Gene: KIF5A

Linked Data

• MyVariant Identifiers: chr12:g.57975653C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57581870C>T , CM000674.2:g.57581870C>T	GRCh38
NC_000012.11:g.57975653C>T , CM000674.1:g.57975653C>T	GRCh37
NC_000012.10:g.56261920C>T	NCBI36
NG_008155.1:g.36807C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.2910C>T MANE Select	ENSP00000408979.2:p.Tyr970=
ENST00000674619.1:c.2931C>T	ENSP00000502270.1:p.Tyr977=
ENST00000675697.1:c.1C>T
ENST00000675737.1:n.314C>T
ENST00000675882.1:n.2433C>T
ENST00000675929.1:n.1468C>T
ENST00000676055.1:c.1C>T
ENST00000676457.1:c.2805C>T	ENSP00000501588.1:p.Tyr935=
ENST00000286452.5:c.2643C>T	ENSP00000286452.5:p.Tyr881=
ENST00000455537.6:c.2910C>T	ENSP00000408979.2:p.Tyr970=
ENST00000552227.1:n.193C>T
NM_004984.2:c.2910C>T	NP_004975.2:p.Tyr970=
NM_001354705.1:c.2643C>T	NP_001341634.1:p.Tyr881=
NM_004984.3:c.2910C>T	NP_004975.2:p.Tyr970=
XR_002957324.1:n.3143C>T
NM_004984.4:c.2910C>T MANE Select	NP_004975.2:p.Tyr970=
NM_001354705.2:c.2643C>T	NP_001341634.1:p.Tyr881=