Canonical Allele Identifier: CA480266241
Gene: KIF5A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.57975692T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57581909T>C , CM000674.2:g.57581909T>C GRCh38
NC_000012.11:g.57975692T>C , CM000674.1:g.57975692T>C GRCh37
NC_000012.10:g.56261959T>C NCBI36
NG_008155.1:g.36846T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000455537.7:c.2949T>C MANE Select ENSP00000408979.2:p.Ser983=
ENST00000674619.1:c.2970T>C ENSP00000502270.1:p.Ser990=
ENST00000675697.1:c.40T>C
ENST00000675737.1:n.353T>C
ENST00000675882.1:n.2472T>C
ENST00000675929.1:n.1507T>C
ENST00000676055.1:c.40T>C
ENST00000676457.1:c.2844T>C ENSP00000501588.1:p.Ser948=
ENST00000286452.5:c.2682T>C ENSP00000286452.5:p.Ser894=
ENST00000455537.6:c.2949T>C ENSP00000408979.2:p.Ser983=
ENST00000552227.1:n.232T>C
NM_004984.2:c.2949T>C NP_004975.2:p.Ser983=
NM_001354705.1:c.2682T>C NP_001341634.1:p.Ser894=
NM_004984.3:c.2949T>C NP_004975.2:p.Ser983=
XR_002957324.1:n.3182T>C
NM_004984.4:c.2949T>C MANE Select NP_004975.2:p.Ser983=
NM_001354705.2:c.2682T>C NP_001341634.1:p.Ser894=