Canonical Allele Identifier: CA480266256

Gene: KIF5A

Linked Data

• MyVariant Identifiers: chr12:g.57975710C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57581927C>T , CM000674.2:g.57581927C>T	GRCh38
NC_000012.11:g.57975710C>T , CM000674.1:g.57975710C>T	GRCh37
NC_000012.10:g.56261977C>T	NCBI36
NG_008155.1:g.36864C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.2967C>T MANE Select	ENSP00000408979.2:p.Ser989=
ENST00000674619.1:c.2988C>T	ENSP00000502270.1:p.Ser996=
ENST00000675697.1:c.58C>T
ENST00000675737.1:n.371C>T
ENST00000675882.1:n.2490C>T
ENST00000675929.1:n.1525C>T
ENST00000676055.1:c.58C>T
ENST00000676457.1:c.2862C>T	ENSP00000501588.1:p.Ser954=
ENST00000286452.5:c.2700C>T	ENSP00000286452.5:p.Ser900=
ENST00000455537.6:c.2967C>T	ENSP00000408979.2:p.Ser989=
ENST00000552227.1:n.250C>T
NM_004984.2:c.2967C>T	NP_004975.2:p.Ser989=
NM_001354705.1:c.2700C>T	NP_001341634.1:p.Ser900=
NM_004984.3:c.2967C>T	NP_004975.2:p.Ser989=
XR_002957324.1:n.3200C>T
NM_004984.4:c.2967C>T MANE Select	NP_004975.2:p.Ser989=
NM_001354705.2:c.2700C>T	NP_001341634.1:p.Ser900=