Canonical Allele Identifier: CA144768

Linked Data

ClinVar Variation Id: 65401
dbSNP Id: rs587777034

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.62361319G>A , CM000667.2:g.62361319G>A GRCh38
NC_000005.9:g.61657146G>A , CM000667.1:g.61657146G>A GRCh37
NC_000005.8:g.61692903G>A NCBI36
NG_042185.1:g.60158G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381103.7:c.869G>A (KIF2A) ENSP00000370493.3:p.Ser290Asn
ENST00000407818.8:c.950G>A (KIF2A) MANE Select ENSP00000385000.3:p.Ser317Asn
ENST00000514082.6:c.950G>A (KIF2A) ENSP00000423542.2:p.Ser317Asn
ENST00000651114.1:c.*183-6971C>T (DIMT1) ENSP00000498538.1:n.*183-6971C>T
ENST00000674632.1:c.893G>A (KIF2A) ENSP00000502498.1:p.Ser298Asn
ENST00000674733.1:c.869G>A (KIF2A) ENSP00000502097.1:p.Ser290Asn
ENST00000674751.1:n.1217G>A (KIF2A)
ENST00000674752.1:c.887G>A (KIF2A) ENSP00000502272.1:p.Ser296Asn
ENST00000674916.1:c.950G>A (KIF2A) ENSP00000502248.1:p.Ser317Asn
ENST00000676122.1:n.1217G>A (KIF2A)
ENST00000676271.1:c.893G>A (KIF2A) ENSP00000501719.1:p.Ser298Asn
ENST00000676413.1:c.869G>A (KIF2A) ENSP00000502125.1:p.Ser290Asn
ENST00000381103.6:c.890G>A (KIF2A) ENSP00000370493.2:p.Ser297Asn
ENST00000401507.7:c.950G>A (KIF2A) ENSP00000385622.3:p.Ser317Asn
ENST00000407818.7:c.950G>A (KIF2A) ENSP00000385000.3:p.Ser317Asn
ENST00000506857.5:c.812G>A (KIF2A) ENSP00000423772.1:p.Ser271Asn
ENST00000509663.2:n.331+54783G>A (KIF2A)
ENST00000512006.2:c.14G>A (KIF2A) ENSP00000421041.2:p.Ser5Asn
NM_001098511.2:c.950G>A (KIF2A) NP_001091981.1:p.Ser317Asn
NM_001243952.1:c.890G>A (KIF2A) NP_001230881.1:p.Ser297Asn
NM_001243953.1:c.893G>A (KIF2A) NP_001230882.1:p.Ser298Asn
NM_004520.4:c.950G>A (KIF2A) NP_004511.2:p.Ser317Asn
XR_001742064.2:n.1256G>A (KIF2A)
NM_001098511.3:c.950G>A (KIF2A) MANE Select NP_001091981.1:p.Ser317Asn
NM_001243952.2:c.869G>A (KIF2A) NP_001230881.2:p.Ser290Asn
NM_001243953.2:c.893G>A (KIF2A) NP_001230882.1:p.Ser298Asn
NM_004520.5:c.950G>A (KIF2A) NP_004511.2:p.Ser317Asn