Canonical Allele Identifier: CA2207178
Gene: KIF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240719129G>A , CM000664.2:g.240719129G>A GRCh38
NC_000002.11:g.241658546G>A , CM000664.1:g.241658546G>A GRCh37
NC_000002.10:g.241307219G>A NCBI36
NG_029724.1:g.106079C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320389.12:c.4812C>T ENSP00000322791.8:p.Phe1604=
ENST00000404283.9:c.5115C>T ENSP00000384231.5:p.Phe1705=
ENST00000431776.6:c.1911C>T ENSP00000414613.2:p.Phe637=
ENST00000492812.6:n.3674C>T
ENST00000498729.9:c.5091C>T MANE Select ENSP00000438388.1:p.Phe1697=
ENST00000647731.1:c.4815C>T ENSP00000498099.1:p.Phe1605=
ENST00000647885.1:c.4902C>T ENSP00000497739.1:p.Phe1634=
ENST00000648047.1:c.4050C>T ENSP00000497935.1:p.Phe1350=
ENST00000648129.1:c.5064C>T ENSP00000497293.1:p.Phe1688=
ENST00000648364.1:c.4815C>T ENSP00000498196.1:p.Phe1605=
ENST00000648680.1:c.4842C>T ENSP00000497586.1:p.Phe1614=
ENST00000649096.1:c.4788C>T ENSP00000497030.1:p.Phe1596=
ENST00000649190.1:n.4085C>T
ENST00000649306.1:c.4890C>T ENSP00000497678.1:p.Phe1630=
ENST00000650053.1:c.4788C>T ENSP00000497824.1:p.Phe1596=
ENST00000650130.1:c.5064C>T ENSP00000498082.1:p.Phe1688=
ENST00000650430.1:n.4163C>T
ENST00000320389.11:c.4788C>T ENSP00000322791.7:p.Phe1596=
ENST00000460788.5:n.1648C>T
ENST00000492812.5:n.1563C>T
ENST00000498729.6:c.5091C>T ENSP00000438388.1:p.Phe1697=
NM_001244008.1:c.5091C>T NP_001230937.1:p.Phe1697=
NM_004321.6:c.4788C>T NP_004312.2:p.Phe1596=
XM_005247022.1:c.5118C>T XP_005247079.1:p.Phe1706=
XM_005247023.1:c.5115C>T XP_005247080.1:p.Phe1705=
XM_005247024.1:c.5091C>T XP_005247081.1:p.Phe1697=
XM_005247026.1:c.4815C>T XP_005247083.1:p.Phe1605=
XM_005247027.1:c.4812C>T XP_005247084.1:p.Phe1604=
XM_005247028.1:c.4788C>T XP_005247085.1:p.Phe1596=
XM_006712605.1:c.5064C>T XP_006712668.1:p.Phe1688=
XM_011511364.1:c.5118C>T XP_011509666.1:p.Phe1706=
XM_011511365.1:c.4842C>T XP_011509667.1:p.Phe1614=
XM_011511366.1:c.4113C>T XP_011509668.1:p.Phe1371=
XM_011511367.1:c.4113C>T XP_011509669.1:p.Phe1371=
NM_001320705.1:c.4815C>T NP_001307634.1:p.Phe1605=
NM_001330289.1:c.4842C>T NP_001317218.1:p.Phe1614=
NM_001330290.1:c.4890C>T NP_001317219.1:p.Phe1630=
NM_004321.7:c.4788C>T NP_004312.2:p.Phe1596=
NM_001320705.2:c.4815C>T NP_001307634.1:p.Phe1605=
NM_001330289.2:c.4842C>T NP_001317218.1:p.Phe1614=
NM_001330290.2:c.4890C>T NP_001317219.1:p.Phe1630=
NM_001244008.2:c.5091C>T MANE Select NP_001230937.1:p.Phe1697=
NM_001379631.1:c.5166C>T NP_001366560.1:p.Phe1722=
NM_001379632.1:c.5067C>T NP_001366561.1:p.Phe1689=
NM_001379633.1:c.5064C>T NP_001366562.1:p.Phe1688=
NM_001379634.1:c.4917C>T NP_001366563.1:p.Phe1639=
NM_001379635.1:c.4914C>T NP_001366564.1:p.Phe1638=
NM_001379636.1:c.4902C>T NP_001366565.1:p.Phe1634=
NM_001379637.1:c.4863C>T NP_001366566.1:p.Phe1621=
NM_001379638.1:c.4839C>T NP_001366567.1:p.Phe1613=
NM_001379639.1:c.4812C>T NP_001366568.1:p.Phe1604=
NM_001379640.1:c.4785C>T NP_001366569.1:p.Phe1595=
NM_001379641.1:c.4788C>T NP_001366570.1:p.Phe1596=
NM_001379642.1:c.5091C>T NP_001366571.1:p.Phe1697=
NM_001379645.1:c.5064C>T NP_001366574.1:p.Phe1688=
NM_001379646.1:c.4914C>T NP_001366575.1:p.Phe1638=
NM_001379648.1:c.4890C>T NP_001366577.1:p.Phe1630=
NM_001379649.1:c.4815C>T NP_001366578.1:p.Phe1605=
NM_001379650.1:c.4788C>T NP_001366579.1:p.Phe1596=
NM_001379651.1:c.4788C>T NP_001366580.1:p.Phe1596=
NM_001379653.1:c.4788C>T NP_001366582.1:p.Phe1596=
NM_004321.8:c.4788C>T NP_004312.2:p.Phe1596=