Canonical Allele Identifier: CA385516609

Gene: KIF5A

Linked Data

• MyVariant Identifiers: chr12:g.57975679G>T (hg19) ; chr12:g.57581896G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57581896G>T , CM000674.2:g.57581896G>T	GRCh38
NC_000012.11:g.57975679G>T , CM000674.1:g.57975679G>T	GRCh37
NC_000012.10:g.56261946G>T	NCBI36
NG_008155.1:g.36833G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.2936G>T MANE Select	ENSP00000408979.2:p.Gly979Val
ENST00000674619.1:c.2957G>T	ENSP00000502270.1:p.Gly986Val
ENST00000675697.1:c.27G>T
ENST00000675737.1:n.340G>T
ENST00000675882.1:n.2459G>T
ENST00000675929.1:n.1494G>T
ENST00000676055.1:c.27G>T
ENST00000676457.1:c.2831G>T	ENSP00000501588.1:p.Gly944Val
ENST00000286452.5:c.2669G>T	ENSP00000286452.5:p.Gly890Val
ENST00000455537.6:c.2936G>T	ENSP00000408979.2:p.Gly979Val
ENST00000552227.1:n.219G>T
NM_004984.2:c.2936G>T	NP_004975.2:p.Gly979Val
NM_001354705.1:c.2669G>T	NP_001341634.1:p.Gly890Val
NM_004984.3:c.2936G>T	NP_004975.2:p.Gly979Val
XR_002957324.1:n.3169G>T
NM_004984.4:c.2936G>T MANE Select	NP_004975.2:p.Gly979Val
NM_001354705.2:c.2669G>T	NP_001341634.1:p.Gly890Val