Canonical Allele Identifier: CA2038922473

Gene: KIF5A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57567887_57567890delinsCTTT , CM000674.2:g.57567887_57567890delinsCTTT	GRCh38
NC_000012.11:g.57961670_57961673delinsCTTT , CM000674.1:g.57961670_57961673delinsCTTT	GRCh37
NC_000012.10:g.56247937_56247940delinsCTTT	NCBI36
NG_008155.1:g.22824_22827delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455537.7:c.714+269_714+272delinsCTTT MANE Select	ENSP00000408979.2:n.714+269_714+272delinsCTTT
ENST00000674619.1:c.714+269_714+272delinsCTTT	ENSP00000502270.1:n.714+269_714+272delinsCTTT
ENST00000676457.1:c.609+269_609+272delinsCTTT	ENSP00000501588.1:n.609+269_609+272delinsCTTT
ENST00000286452.5:c.447+269_447+272delinsCTTT	ENSP00000286452.5:n.447+269_447+272delinsCTTT
ENST00000455537.6:c.714+269_714+272delinsCTTT	ENSP00000408979.2:n.714+269_714+272delinsCTTT
NM_004984.2:c.714+269_714+272delinsCTTT	NP_004975.2:n.714+269_714+272delinsCTTT
NM_001354705.1:c.447+269_447+272delinsCTTT	NP_001341634.1:n.447+269_447+272delinsCTTT
NM_004984.3:c.714+269_714+272delinsCTTT	NP_004975.2:n.714+269_714+272delinsCTTT
XR_002957324.1:n.947+269_947+272delinsCTTT
NM_004984.4:c.714+269_714+272delinsCTTT MANE Select	NP_004975.2:n.714+269_714+272delinsCTTT
NM_001354705.2:c.447+269_447+272delinsCTTT	NP_001341634.1:n.447+269_447+272delinsCTTT