Canonical Allele Identifier: CA2038921948

Gene: KIF5A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57567661_57567664delinsCTTT , CM000674.2:g.57567661_57567664delinsCTTT	GRCh38
NC_000012.11:g.57961444_57961447delinsCTTT , CM000674.1:g.57961444_57961447delinsCTTT	GRCh37
NC_000012.10:g.56247711_56247714delinsCTTT	NCBI36
NG_008155.1:g.22598_22601delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.714+43_714+46delinsCTTT MANE Select	ENSP00000408979.2:n.714+43_714+46delinsCTTT
ENST00000674619.1:c.714+43_714+46delinsCTTT	ENSP00000502270.1:n.714+43_714+46delinsCTTT
ENST00000676457.1:c.609+43_609+46delinsCTTT	ENSP00000501588.1:n.609+43_609+46delinsCTTT
ENST00000286452.5:c.447+43_447+46delinsCTTT	ENSP00000286452.5:n.447+43_447+46delinsCTTT
ENST00000455537.6:c.714+43_714+46delinsCTTT	ENSP00000408979.2:n.714+43_714+46delinsCTTT
NM_004984.2:c.714+43_714+46delinsCTTT	NP_004975.2:n.714+43_714+46delinsCTTT
NM_001354705.1:c.447+43_447+46delinsCTTT	NP_001341634.1:n.447+43_447+46delinsCTTT
NM_004984.3:c.714+43_714+46delinsCTTT	NP_004975.2:n.714+43_714+46delinsCTTT
XR_002957324.1:n.947+43_947+46delinsCTTT
NM_004984.4:c.714+43_714+46delinsCTTT MANE Select	NP_004975.2:n.714+43_714+46delinsCTTT
NM_001354705.2:c.447+43_447+46delinsCTTT	NP_001341634.1:n.447+43_447+46delinsCTTT