Canonical Allele Identifier: CA2207162

Gene: KIF1A

Linked Data

• ClinVar Variation Id: 464259
• ClinVar RCV Id: RCV000719407 ; RCV000757422 ; RCV001088413 ; RCV001141523 ; RCV004541687
• dbSNP Id: rs200511467
• ExAC: 2:241658482 C / T
• gnomAD v2: 2-241658482-C-T
• gnomAD v3: 2-240719065-C-T
• gnomAD v4: 2-240719065-C-T
• MyVariant Identifiers: chr2:g.241658482C>T (hg19) ; chr2:g.240719065C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240719065C>T , CM000664.2:g.240719065C>T	GRCh38
NC_000002.11:g.241658482C>T , CM000664.1:g.241658482C>T	GRCh37
NC_000002.10:g.241307155C>T	NCBI36
NG_029724.1:g.106143G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320389.12:c.4876G>A	ENSP00000322791.8:p.Val1626Met
ENST00000404283.9:c.5179G>A	ENSP00000384231.5:p.Val1727Met
ENST00000431776.6:c.1975G>A	ENSP00000414613.2:p.Val659Met
ENST00000492812.6:n.3738G>A
ENST00000498729.9:c.5155G>A MANE Select	ENSP00000438388.1:p.Val1719Met
ENST00000647731.1:c.4879G>A	ENSP00000498099.1:p.Val1627Met
ENST00000647885.1:c.4966G>A	ENSP00000497739.1:p.Val1656Met
ENST00000648047.1:c.4114G>A	ENSP00000497935.1:p.Val1372Met
ENST00000648129.1:c.5128G>A	ENSP00000497293.1:p.Val1710Met
ENST00000648364.1:c.4879G>A	ENSP00000498196.1:p.Val1627Met
ENST00000648680.1:c.4906G>A	ENSP00000497586.1:p.Val1636Met
ENST00000649096.1:c.4852G>A	ENSP00000497030.1:p.Val1618Met
ENST00000649190.1:n.4149G>A
ENST00000649306.1:c.4954G>A	ENSP00000497678.1:p.Val1652Met
ENST00000650053.1:c.4852G>A	ENSP00000497824.1:p.Val1618Met
ENST00000650130.1:c.5128G>A	ENSP00000498082.1:p.Val1710Met
ENST00000650430.1:n.4227G>A
ENST00000320389.11:c.4852G>A	ENSP00000322791.7:p.Val1618Met
ENST00000460788.5:n.1712G>A
ENST00000492812.5:n.1627G>A
ENST00000498729.6:c.5155G>A	ENSP00000438388.1:p.Val1719Met
NM_001244008.1:c.5155G>A	NP_001230937.1:p.Val1719Met
NM_004321.6:c.4852G>A	NP_004312.2:p.Val1618Met
XM_005247022.1:c.5182G>A	XP_005247079.1:p.Val1728Met
XM_005247023.1:c.5179G>A	XP_005247080.1:p.Val1727Met
XM_005247024.1:c.5155G>A	XP_005247081.1:p.Val1719Met
XM_005247026.1:c.4879G>A	XP_005247083.1:p.Val1627Met
XM_005247027.1:c.4876G>A	XP_005247084.1:p.Val1626Met
XM_005247028.1:c.4852G>A	XP_005247085.1:p.Val1618Met
XM_006712605.1:c.5128G>A	XP_006712668.1:p.Val1710Met
XM_011511364.1:c.5182G>A	XP_011509666.1:p.Val1728Met
XM_011511365.1:c.4906G>A	XP_011509667.1:p.Val1636Met
XM_011511366.1:c.4177G>A	XP_011509668.1:p.Val1393Met
XM_011511367.1:c.4177G>A	XP_011509669.1:p.Val1393Met
NM_001320705.1:c.4879G>A	NP_001307634.1:p.Val1627Met
NM_001330289.1:c.4906G>A	NP_001317218.1:p.Val1636Met
NM_001330290.1:c.4954G>A	NP_001317219.1:p.Val1652Met
NM_004321.7:c.4852G>A	NP_004312.2:p.Val1618Met
NM_001320705.2:c.4879G>A	NP_001307634.1:p.Val1627Met
NM_001330289.2:c.4906G>A	NP_001317218.1:p.Val1636Met
NM_001330290.2:c.4954G>A	NP_001317219.1:p.Val1652Met
NM_001244008.2:c.5155G>A MANE Select	NP_001230937.1:p.Val1719Met
NM_001379631.1:c.5230G>A	NP_001366560.1:p.Val1744Met
NM_001379632.1:c.5131G>A	NP_001366561.1:p.Val1711Met
NM_001379633.1:c.5128G>A	NP_001366562.1:p.Val1710Met
NM_001379634.1:c.4981G>A	NP_001366563.1:p.Val1661Met
NM_001379635.1:c.4978G>A	NP_001366564.1:p.Val1660Met
NM_001379636.1:c.4966G>A	NP_001366565.1:p.Val1656Met
NM_001379637.1:c.4927G>A	NP_001366566.1:p.Val1643Met
NM_001379638.1:c.4903G>A	NP_001366567.1:p.Val1635Met
NM_001379639.1:c.4876G>A	NP_001366568.1:p.Val1626Met
NM_001379640.1:c.4849G>A	NP_001366569.1:p.Val1617Met
NM_001379641.1:c.4852G>A	NP_001366570.1:p.Val1618Met
NM_001379642.1:c.5155G>A	NP_001366571.1:p.Val1719Met
NM_001379645.1:c.5128G>A	NP_001366574.1:p.Val1710Met
NM_001379646.1:c.4978G>A	NP_001366575.1:p.Val1660Met
NM_001379648.1:c.4954G>A	NP_001366577.1:p.Val1652Met
NM_001379649.1:c.4879G>A	NP_001366578.1:p.Val1627Met
NM_001379650.1:c.4852G>A	NP_001366579.1:p.Val1618Met
NM_001379651.1:c.4852G>A	NP_001366580.1:p.Val1618Met
NM_001379653.1:c.4852G>A	NP_001366582.1:p.Val1618Met
NM_004321.8:c.4852G>A	NP_004312.2:p.Val1618Met