Canonical Allele Identifier: CA144766

Linked Data

ClinVar Variation Id: 65400
ClinVar RCV Id: RCV000055623
dbSNP Id: rs587777033

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.62361330C>G , CM000667.2:g.62361330C>G GRCh38
NC_000005.9:g.61657157C>G , CM000667.1:g.61657157C>G GRCh37
NC_000005.8:g.61692914C>G NCBI36
NG_042185.1:g.60169C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381103.7:c.880C>G (KIF2A) ENSP00000370493.3:p.His294Asp
ENST00000407818.8:c.961C>G (KIF2A) MANE Select ENSP00000385000.3:p.His321Asp
ENST00000514082.6:c.961C>G (KIF2A) ENSP00000423542.2:p.His321Asp
ENST00000651114.1:c.*183-6982G>C (DIMT1) ENSP00000498538.1:n.*183-6982G>C
ENST00000674632.1:c.904C>G (KIF2A) ENSP00000502498.1:p.His302Asp
ENST00000674733.1:c.880C>G (KIF2A) ENSP00000502097.1:p.His294Asp
ENST00000674751.1:n.1228C>G (KIF2A)
ENST00000674752.1:c.898C>G (KIF2A) ENSP00000502272.1:p.His300Asp
ENST00000674916.1:c.961C>G (KIF2A) ENSP00000502248.1:p.His321Asp
ENST00000676122.1:n.1228C>G (KIF2A)
ENST00000676271.1:c.904C>G (KIF2A) ENSP00000501719.1:p.His302Asp
ENST00000676413.1:c.880C>G (KIF2A) ENSP00000502125.1:p.His294Asp
ENST00000381103.6:c.901C>G (KIF2A) ENSP00000370493.2:p.His301Asp
ENST00000401507.7:c.961C>G (KIF2A) ENSP00000385622.3:p.His321Asp
ENST00000407818.7:c.961C>G (KIF2A) ENSP00000385000.3:p.His321Asp
ENST00000506857.5:c.823C>G (KIF2A) ENSP00000423772.1:p.His275Asp
ENST00000509663.2:n.331+54794C>G (KIF2A)
ENST00000512006.2:c.25C>G (KIF2A) ENSP00000421041.2:p.His9Asp
NM_001098511.2:c.961C>G (KIF2A) NP_001091981.1:p.His321Asp
NM_001243952.1:c.901C>G (KIF2A) NP_001230881.1:p.His301Asp
NM_001243953.1:c.904C>G (KIF2A) NP_001230882.1:p.His302Asp
NM_004520.4:c.961C>G (KIF2A) NP_004511.2:p.His321Asp
XR_001742064.2:n.1267C>G (KIF2A)
NM_001098511.3:c.961C>G (KIF2A) MANE Select NP_001091981.1:p.His321Asp
NM_001243952.2:c.880C>G (KIF2A) NP_001230881.2:p.His294Asp
NM_001243953.2:c.904C>G (KIF2A) NP_001230882.1:p.His302Asp
NM_004520.5:c.961C>G (KIF2A) NP_004511.2:p.His321Asp