Canonical Allele Identifier: CA385516622

Gene: KIF5A

Linked Data

• MyVariant Identifiers: chr12:g.57975684A>C (hg19) ; chr12:g.57581901A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57581901A>C , CM000674.2:g.57581901A>C	GRCh38
NC_000012.11:g.57975684A>C , CM000674.1:g.57975684A>C	GRCh37
NC_000012.10:g.56261951A>C	NCBI36
NG_008155.1:g.36838A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.2941A>C MANE Select	ENSP00000408979.2:p.Thr981Pro
ENST00000674619.1:c.2962A>C	ENSP00000502270.1:p.Thr988Pro
ENST00000675697.1:c.32A>C
ENST00000675737.1:n.345A>C
ENST00000675882.1:n.2464A>C
ENST00000675929.1:n.1499A>C
ENST00000676055.1:c.32A>C
ENST00000676457.1:c.2836A>C	ENSP00000501588.1:p.Thr946Pro
ENST00000286452.5:c.2674A>C	ENSP00000286452.5:p.Thr892Pro
ENST00000455537.6:c.2941A>C	ENSP00000408979.2:p.Thr981Pro
ENST00000552227.1:n.224A>C
NM_004984.2:c.2941A>C	NP_004975.2:p.Thr981Pro
NM_001354705.1:c.2674A>C	NP_001341634.1:p.Thr892Pro
NM_004984.3:c.2941A>C	NP_004975.2:p.Thr981Pro
XR_002957324.1:n.3174A>C
NM_004984.4:c.2941A>C MANE Select	NP_004975.2:p.Thr981Pro
NM_001354705.2:c.2674A>C	NP_001341634.1:p.Thr892Pro