Canonical Allele Identifier: CA385516562

Gene: KIF5A

Linked Data

• COSMIC: COSM381894
• MyVariant Identifiers: chr12:g.57975667G>C (hg19) ; chr12:g.57581884G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57581884G>C , CM000674.2:g.57581884G>C	GRCh38
NC_000012.11:g.57975667G>C , CM000674.1:g.57975667G>C	GRCh37
NC_000012.10:g.56261934G>C	NCBI36
NG_008155.1:g.36821G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.2924G>C MANE Select	ENSP00000408979.2:p.Cys975Ser
ENST00000674619.1:c.2945G>C	ENSP00000502270.1:p.Cys982Ser
ENST00000675697.1:c.15G>C
ENST00000675737.1:n.328G>C
ENST00000675882.1:n.2447G>C
ENST00000675929.1:n.1482G>C
ENST00000676055.1:c.15G>C
ENST00000676457.1:c.2819G>C	ENSP00000501588.1:p.Cys940Ser
ENST00000286452.5:c.2657G>C	ENSP00000286452.5:p.Cys886Ser
ENST00000455537.6:c.2924G>C	ENSP00000408979.2:p.Cys975Ser
ENST00000552227.1:n.207G>C
NM_004984.2:c.2924G>C	NP_004975.2:p.Cys975Ser
NM_001354705.1:c.2657G>C	NP_001341634.1:p.Cys886Ser
NM_004984.3:c.2924G>C	NP_004975.2:p.Cys975Ser
XR_002957324.1:n.3157G>C
NM_004984.4:c.2924G>C MANE Select	NP_004975.2:p.Cys975Ser
NM_001354705.2:c.2657G>C	NP_001341634.1:p.Cys886Ser