Canonical Allele Identifier: CA237787513

Gene: KIF5A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57576541C>G , CM000674.2:g.57576541C>G	GRCh38
NC_000012.11:g.57970324C>G , CM000674.1:g.57970324C>G	GRCh37
NC_000012.10:g.56256591C>G	NCBI36
NG_008155.1:g.31478C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004984.4:c.2198+163C>G MANE Select	NP_004975.2:n.2198+163C>G
ENST00000455537.7:c.2198+163C>G MANE Select	ENSP00000408979.2:n.2198+163C>G
NM_001354705.1:c.1931+163C>G	NP_001341634.1:n.1931+163C>G
NM_001354705.2:c.1931+163C>G	NP_001341634.1:n.1931+163C>G
NM_004984.2:c.2198+163C>G	NP_004975.2:n.2198+163C>G
NM_004984.3:c.2198+163C>G	NP_004975.2:n.2198+163C>G
ENST00000286452.5:c.1931+163C>G	ENSP00000286452.5:n.1931+163C>G
ENST00000455537.6:c.2198+163C>G	ENSP00000408979.2:n.2198+163C>G
ENST00000674619.1:c.2198+163C>G	ENSP00000502270.1:n.2198+163C>G
ENST00000675299.1:c.346+163C>G	ENSP00000501888.1:n.346+163C>G
ENST00000675882.1:n.1185+163C>G
ENST00000675929.1:n.756+163C>G
ENST00000675984.1:n.2049C>G
ENST00000676081.1:n.1624C>G
ENST00000676457.1:c.2093+163C>G	ENSP00000501588.1:n.2093+163C>G
XR_002957324.1:n.2431+163C>G