Canonical Allele Identifier: CA2038911119
Gene: KIF5A HGNC NCBI

Linked Data

dbSNP Id: rs1882627167

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57582171G>A , CM000674.2:g.57582171G>A GRCh38
NC_000012.11:g.57975954G>A , CM000674.1:g.57975954G>A GRCh37
NC_000012.10:g.56262221G>A NCBI36
NG_008155.1:g.37108G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.2992+219G>A MANE Select ENSP00000408979.2:n.2992+219G>A
ENST00000674619.1:c.3013+219G>A ENSP00000502270.1:n.3013+219G>A
ENST00000675697.1:c.83+219G>A
ENST00000675737.1:n.615G>A
ENST00000675882.1:n.2515+219G>A
ENST00000675929.1:n.1550+219G>A
ENST00000676055.1:c.83+219G>A
ENST00000676437.1:c.17+219G>A
ENST00000676457.1:c.2887+219G>A ENSP00000501588.1:n.2887+219G>A
ENST00000286452.5:c.2725+219G>A ENSP00000286452.5:n.2725+219G>A
ENST00000455537.6:c.2992+219G>A ENSP00000408979.2:n.2992+219G>A
ENST00000552227.1:n.275+219G>A
NM_004984.2:c.2992+219G>A NP_004975.2:n.2992+219G>A
NM_001354705.1:c.2725+219G>A NP_001341634.1:n.2725+219G>A
NM_004984.3:c.2992+219G>A NP_004975.2:n.2992+219G>A
XR_002957324.1:n.3225+219G>A
NM_004984.4:c.2992+219G>A MANE Select NP_004975.2:n.2992+219G>A
NM_001354705.2:c.2725+219G>A NP_001341634.1:n.2725+219G>A