Canonical Allele Identifier: CA2207399
Community Standard Title: NM_001244008.2(KIF1A):c.4498G>C (p.Glu1500Gln)
Gene: KIF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240722623C>G , CM000664.2:g.240722623C>G GRCh38
NC_000002.11:g.241662040C>G , CM000664.1:g.241662040C>G GRCh37
NC_000002.10:g.241310713C>G NCBI36
NG_029724.1:g.102585G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001244008.2:c.4498G>C MANE Select NP_001230937.1:p.Glu1500Gln
ENST00000498729.9:c.4498G>C MANE Select ENSP00000438388.1:p.Glu1500Gln
NM_001244008.1:c.4498G>C NP_001230937.1:p.Glu1500Gln
NM_001320705.1:c.4222G>C NP_001307634.1:p.Glu1408Gln
NM_001320705.2:c.4222G>C NP_001307634.1:p.Glu1408Gln
NM_001330289.1:c.4249G>C NP_001317218.1:p.Glu1417Gln
NM_001330289.2:c.4249G>C NP_001317218.1:p.Glu1417Gln
NM_001330290.1:c.4297G>C NP_001317219.1:p.Glu1433Gln
NM_001330290.2:c.4297G>C NP_001317219.1:p.Glu1433Gln
NM_001379631.1:c.4573G>C NP_001366560.1:p.Glu1525Gln
NM_001379632.1:c.4474G>C NP_001366561.1:p.Glu1492Gln
NM_001379633.1:c.4471G>C NP_001366562.1:p.Glu1491Gln
NM_001379634.1:c.4324G>C NP_001366563.1:p.Glu1442Gln
NM_001379635.1:c.4321G>C NP_001366564.1:p.Glu1441Gln
NM_001379636.1:c.4309G>C NP_001366565.1:p.Glu1437Gln
NM_001379637.1:c.4270G>C NP_001366566.1:p.Glu1424Gln
NM_001379638.1:c.4246G>C NP_001366567.1:p.Glu1416Gln
NM_001379639.1:c.4219G>C NP_001366568.1:p.Glu1407Gln
NM_001379640.1:c.4192G>C NP_001366569.1:p.Glu1398Gln
NM_001379641.1:c.4195G>C NP_001366570.1:p.Glu1399Gln
NM_001379642.1:c.4498G>C NP_001366571.1:p.Glu1500Gln
NM_001379645.1:c.4471G>C NP_001366574.1:p.Glu1491Gln
NM_001379646.1:c.4321G>C NP_001366575.1:p.Glu1441Gln
NM_001379648.1:c.4297G>C NP_001366577.1:p.Glu1433Gln
NM_001379649.1:c.4222G>C NP_001366578.1:p.Glu1408Gln
NM_001379650.1:c.4195G>C NP_001366579.1:p.Glu1399Gln
NM_001379651.1:c.4195G>C NP_001366580.1:p.Glu1399Gln
NM_001379653.1:c.4195G>C NP_001366582.1:p.Glu1399Gln
NM_004321.6:c.4195G>C NP_004312.2:p.Glu1399Gln
NM_004321.7:c.4195G>C NP_004312.2:p.Glu1399Gln
NM_004321.8:c.4195G>C NP_004312.2:p.Glu1399Gln
ENST00000320389.11:c.4195G>C ENSP00000322791.7:p.Glu1399Gln
ENST00000320389.12:c.4219G>C ENSP00000322791.8:p.Glu1407Gln
ENST00000404283.9:c.4522G>C ENSP00000384231.5:p.Glu1508Gln
ENST00000431776.5:c.993G>C
ENST00000431776.6:c.1318G>C ENSP00000414613.2:p.Glu440Gln
ENST00000460788.5:n.1055G>C
ENST00000465813.1:n.36G>C
ENST00000465813.2:n.58G>C
ENST00000492812.5:n.970G>C
ENST00000492812.6:n.3081G>C
ENST00000498729.6:c.4498G>C ENSP00000438388.1:p.Glu1500Gln
ENST00000647731.1:c.4222G>C ENSP00000498099.1:p.Glu1408Gln
ENST00000647885.1:c.4309G>C ENSP00000497739.1:p.Glu1437Gln
ENST00000648047.1:c.3457G>C ENSP00000497935.1:p.Glu1153Gln
ENST00000648129.1:c.4471G>C ENSP00000497293.1:p.Glu1491Gln
ENST00000648364.1:c.4222G>C ENSP00000498196.1:p.Glu1408Gln
ENST00000648680.1:c.4249G>C ENSP00000497586.1:p.Glu1417Gln
ENST00000649096.1:c.4195G>C ENSP00000497030.1:p.Glu1399Gln
ENST00000649190.1:n.3492G>C
ENST00000649306.1:c.4297G>C ENSP00000497678.1:p.Glu1433Gln
ENST00000650053.1:c.4195G>C ENSP00000497824.1:p.Glu1399Gln
ENST00000650130.1:c.4471G>C ENSP00000498082.1:p.Glu1491Gln
ENST00000650430.1:n.3570G>C
XM_005247022.1:c.4525G>C XP_005247079.1:p.Glu1509Gln
XM_005247023.1:c.4522G>C XP_005247080.1:p.Glu1508Gln
XM_005247024.1:c.4498G>C XP_005247081.1:p.Glu1500Gln
XM_005247026.1:c.4222G>C XP_005247083.1:p.Glu1408Gln
XM_005247027.1:c.4219G>C XP_005247084.1:p.Glu1407Gln
XM_005247028.1:c.4195G>C XP_005247085.1:p.Glu1399Gln
XM_006712605.1:c.4471G>C XP_006712668.1:p.Glu1491Gln
XM_011511364.1:c.4525G>C XP_011509666.1:p.Glu1509Gln
XM_011511365.1:c.4249G>C XP_011509667.1:p.Glu1417Gln
XM_011511366.1:c.3520G>C XP_011509668.1:p.Glu1174Gln
XM_011511367.1:c.3520G>C XP_011509669.1:p.Glu1174Gln