Canonical Allele Identifier: CA647591275

Gene: KIF1A

Linked Data

• COSMIC: COSN1236516 ; COSN5790706

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240775632C>T , CM000664.2:g.240775632C>T	GRCh38
NC_000002.11:g.241715049C>T , CM000664.1:g.241715049C>T	GRCh37
NC_000002.10:g.241363722C>T	NCBI36
NG_029724.1:g.49576G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320389.12:c.958+219G>A	ENSP00000322791.8:n.958+219G>A
ENST00000404283.9:c.958+219G>A	ENSP00000384231.5:n.958+219G>A
ENST00000428768.2:c.958+219G>A	ENSP00000395443.2:n.958+219G>A
ENST00000498729.9:c.958+219G>A MANE Select	ENSP00000438388.1:n.958+219G>A
ENST00000647731.1:c.958+219G>A	ENSP00000498099.1:n.958+219G>A
ENST00000647885.1:c.958+219G>A	ENSP00000497739.1:n.958+219G>A
ENST00000648047.1:c.94+219G>A	ENSP00000497935.1:n.94+219G>A
ENST00000648129.1:c.958+219G>A	ENSP00000497293.1:n.958+219G>A
ENST00000648364.1:c.958+219G>A	ENSP00000498196.1:n.958+219G>A
ENST00000648534.1:n.151+219G>A
ENST00000648680.1:c.958+219G>A	ENSP00000497586.1:n.958+219G>A
ENST00000648854.1:n.220+219G>A
ENST00000649064.1:n.1116+219G>A
ENST00000649096.1:c.958+219G>A	ENSP00000497030.1:n.958+219G>A
ENST00000649190.1:n.228+219G>A
ENST00000649306.1:c.958+219G>A	ENSP00000497678.1:n.958+219G>A
ENST00000649381.1:n.1109+219G>A
ENST00000650053.1:c.958+219G>A	ENSP00000497824.1:n.958+219G>A
ENST00000650130.1:c.958+219G>A	ENSP00000498082.1:n.958+219G>A
ENST00000650430.1:n.333+219G>A
ENST00000650542.1:n.1333G>A
ENST00000674607.1:c.76+219G>A	ENSP00000501825.1:n.76+219G>A
ENST00000676135.1:n.76+219G>A
ENST00000320389.11:c.958+219G>A	ENSP00000322791.7:n.958+219G>A
ENST00000404283.7:c.958+219G>A	ENSP00000384231.3:n.958+219G>A
ENST00000428768.1:c.380+219G>A
ENST00000498729.6:c.958+219G>A	ENSP00000438388.1:n.958+219G>A
NM_001244008.1:c.958+219G>A	NP_001230937.1:n.958+219G>A
NM_004321.6:c.958+219G>A	NP_004312.2:n.958+219G>A
XM_005247022.1:c.958+219G>A	XP_005247079.1:n.958+219G>A
XM_005247023.1:c.958+219G>A	XP_005247080.1:n.958+219G>A
XM_005247024.1:c.958+219G>A	XP_005247081.1:n.958+219G>A
XM_005247026.1:c.958+219G>A	XP_005247083.1:n.958+219G>A
XM_005247027.1:c.958+219G>A	XP_005247084.1:n.958+219G>A
XM_005247028.1:c.958+219G>A	XP_005247085.1:n.958+219G>A
XM_006712605.1:c.958+219G>A	XP_006712668.1:n.958+219G>A
XM_011511364.1:c.958+219G>A	XP_011509666.1:n.958+219G>A
XM_011511365.1:c.958+219G>A	XP_011509667.1:n.958+219G>A
XM_011511366.1:c.-21+219G>A	XP_011509668.1:n.-21+219G>A
XM_011511367.1:c.-21+219G>A	XP_011509669.1:n.-21+219G>A
NM_001320705.1:c.958+219G>A	NP_001307634.1:n.958+219G>A
NM_001330289.1:c.958+219G>A	NP_001317218.1:n.958+219G>A
NM_001330290.1:c.958+219G>A	NP_001317219.1:n.958+219G>A
NM_004321.7:c.958+219G>A	NP_004312.2:n.958+219G>A
NM_001320705.2:c.958+219G>A	NP_001307634.1:n.958+219G>A
NM_001330289.2:c.958+219G>A	NP_001317218.1:n.958+219G>A
NM_001330290.2:c.958+219G>A	NP_001317219.1:n.958+219G>A
NM_001244008.2:c.958+219G>A MANE Select	NP_001230937.1:n.958+219G>A
NM_001379631.1:c.958+219G>A	NP_001366560.1:n.958+219G>A
NM_001379632.1:c.958+219G>A	NP_001366561.1:n.958+219G>A
NM_001379633.1:c.958+219G>A	NP_001366562.1:n.958+219G>A
NM_001379634.1:c.958+219G>A	NP_001366563.1:n.958+219G>A
NM_001379635.1:c.958+219G>A	NP_001366564.1:n.958+219G>A
NM_001379636.1:c.958+219G>A	NP_001366565.1:n.958+219G>A
NM_001379637.1:c.958+219G>A	NP_001366566.1:n.958+219G>A
NM_001379638.1:c.958+219G>A	NP_001366567.1:n.958+219G>A
NM_001379639.1:c.958+219G>A	NP_001366568.1:n.958+219G>A
NM_001379640.1:c.958+219G>A	NP_001366569.1:n.958+219G>A
NM_001379641.1:c.958+219G>A	NP_001366570.1:n.958+219G>A
NM_001379642.1:c.958+219G>A	NP_001366571.1:n.958+219G>A
NM_001379645.1:c.958+219G>A	NP_001366574.1:n.958+219G>A
NM_001379646.1:c.958+219G>A	NP_001366575.1:n.958+219G>A
NM_001379648.1:c.958+219G>A	NP_001366577.1:n.958+219G>A
NM_001379649.1:c.958+219G>A	NP_001366578.1:n.958+219G>A
NM_001379650.1:c.958+219G>A	NP_001366579.1:n.958+219G>A
NM_001379651.1:c.958+219G>A	NP_001366580.1:n.958+219G>A
NM_001379653.1:c.958+219G>A	NP_001366582.1:n.958+219G>A
NM_004321.8:c.958+219G>A	NP_004312.2:n.958+219G>A