Canonical Allele Identifier: CA2038910745
Gene: KIF5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57581975C= , CM000674.2:g.57581975C= GRCh38
NC_000012.11:g.57975758C= , CM000674.1:g.57975758C= GRCh37
NC_000012.10:g.56262025C= NCBI36
NG_008155.1:g.36912C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.2992+23C= MANE Select ENSP00000408979.2:n.2992+23C=
ENST00000674619.1:c.3013+23C= ENSP00000502270.1:n.3013+23C=
ENST00000675697.1:c.83+23C=
ENST00000675737.1:n.419C=
ENST00000675882.1:n.2515+23C=
ENST00000675929.1:n.1550+23C=
ENST00000676055.1:c.83+23C=
ENST00000676437.1:c.17+23C=
ENST00000676457.1:c.2887+23C= ENSP00000501588.1:n.2887+23C=
ENST00000286452.5:c.2725+23C= ENSP00000286452.5:n.2725+23C=
ENST00000455537.6:c.2992+23C= ENSP00000408979.2:n.2992+23C=
ENST00000552227.1:n.275+23C=
NM_004984.2:c.2992+23C= NP_004975.2:n.2992+23C=
NM_001354705.1:c.2725+23C= NP_001341634.1:n.2725+23C=
NM_004984.3:c.2992+23C= NP_004975.2:n.2992+23C=
XR_002957324.1:n.3225+23C=
NM_004984.4:c.2992+23C= MANE Select NP_004975.2:n.2992+23C=
NM_001354705.2:c.2725+23C= NP_001341634.1:n.2725+23C=