Canonical Allele Identifier: CA351328607

Gene: KIF1A

Linked Data

• MyVariant Identifiers: chr2:g.241706740T>G (hg19) ; chr2:g.240767323T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240767323T>G , CM000664.2:g.240767323T>G	GRCh38
NC_000002.11:g.241706740T>G , CM000664.1:g.241706740T>G	GRCh37
NC_000002.10:g.241355413T>G	NCBI36
NG_029724.1:g.57885A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000320389.12:c.1493A>C	ENSP00000322791.8:p.Asn498Thr
ENST00000404283.9:c.1520A>C	ENSP00000384231.5:p.Asn507Thr
ENST00000498729.9:c.1520A>C MANE Select	ENSP00000438388.1:p.Asn507Thr
ENST00000647731.1:c.1493A>C	ENSP00000498099.1:p.Asn498Thr
ENST00000647885.1:c.1493A>C	ENSP00000497739.1:p.Asn498Thr
ENST00000648047.1:c.731A>C	ENSP00000497935.1:p.Asn244Thr
ENST00000648129.1:c.1493A>C	ENSP00000497293.1:p.Asn498Thr
ENST00000648364.1:c.1520A>C	ENSP00000498196.1:p.Asn507Thr
ENST00000648680.1:c.1520A>C	ENSP00000497586.1:p.Asn507Thr
ENST00000649064.1:n.1651A>C
ENST00000649096.1:c.1493A>C	ENSP00000497030.1:p.Asn498Thr
ENST00000649190.1:n.790A>C
ENST00000649306.1:c.1595A>C	ENSP00000497678.1:p.Asn532Thr
ENST00000649381.1:n.1746A>C
ENST00000650053.1:c.1493A>C	ENSP00000497824.1:p.Asn498Thr
ENST00000650130.1:c.1493A>C	ENSP00000498082.1:p.Asn498Thr
ENST00000650430.1:n.868A>C
ENST00000320389.11:c.1493A>C	ENSP00000322791.7:p.Asn498Thr
ENST00000404283.7:c.1520A>C	ENSP00000384231.3:p.Asn507Thr
ENST00000498729.6:c.1520A>C	ENSP00000438388.1:p.Asn507Thr
NM_001244008.1:c.1520A>C	NP_001230937.1:p.Asn507Thr
NM_004321.6:c.1493A>C	NP_004312.2:p.Asn498Thr
XM_005247022.1:c.1520A>C	XP_005247079.1:p.Asn507Thr
XM_005247023.1:c.1520A>C	XP_005247080.1:p.Asn507Thr
XM_005247024.1:c.1493A>C	XP_005247081.1:p.Asn498Thr
XM_005247026.1:c.1520A>C	XP_005247083.1:p.Asn507Thr
XM_005247027.1:c.1493A>C	XP_005247084.1:p.Asn498Thr
XM_005247028.1:c.1493A>C	XP_005247085.1:p.Asn498Thr
XM_006712605.1:c.1493A>C	XP_006712668.1:p.Asn498Thr
XM_011511364.1:c.1520A>C	XP_011509666.1:p.Asn507Thr
XM_011511365.1:c.1520A>C	XP_011509667.1:p.Asn507Thr
XM_011511366.1:c.515A>C	XP_011509668.1:p.Asn172Thr
XM_011511367.1:c.515A>C	XP_011509669.1:p.Asn172Thr
NM_001320705.1:c.1520A>C	NP_001307634.1:p.Asn507Thr
NM_001330289.1:c.1520A>C	NP_001317218.1:p.Asn507Thr
NM_001330290.1:c.1595A>C	NP_001317219.1:p.Asn532Thr
NM_004321.7:c.1493A>C	NP_004312.2:p.Asn498Thr
NM_001320705.2:c.1520A>C	NP_001307634.1:p.Asn507Thr
NM_001330289.2:c.1520A>C	NP_001317218.1:p.Asn507Thr
NM_001330290.2:c.1595A>C	NP_001317219.1:p.Asn532Thr
NM_001244008.2:c.1520A>C MANE Select	NP_001230937.1:p.Asn507Thr
NM_001379631.1:c.1595A>C	NP_001366560.1:p.Asn532Thr
NM_001379632.1:c.1493A>C	NP_001366561.1:p.Asn498Thr
NM_001379633.1:c.1493A>C	NP_001366562.1:p.Asn498Thr
NM_001379634.1:c.1595A>C	NP_001366563.1:p.Asn532Thr
NM_001379635.1:c.1595A>C	NP_001366564.1:p.Asn532Thr
NM_001379636.1:c.1493A>C	NP_001366565.1:p.Asn498Thr
NM_001379637.1:c.1568A>C	NP_001366566.1:p.Asn523Thr
NM_001379638.1:c.1520A>C	NP_001366567.1:p.Asn507Thr
NM_001379639.1:c.1493A>C	NP_001366568.1:p.Asn498Thr
NM_001379640.1:c.1493A>C	NP_001366569.1:p.Asn498Thr
NM_001379641.1:c.1493A>C	NP_001366570.1:p.Asn498Thr
NM_001379642.1:c.1493A>C	NP_001366571.1:p.Asn498Thr
NM_001379645.1:c.1493A>C	NP_001366574.1:p.Asn498Thr
NM_001379646.1:c.1595A>C	NP_001366575.1:p.Asn532Thr
NM_001379648.1:c.1568A>C	NP_001366577.1:p.Asn523Thr
NM_001379649.1:c.1493A>C	NP_001366578.1:p.Asn498Thr
NM_001379650.1:c.1493A>C	NP_001366579.1:p.Asn498Thr
NM_001379651.1:c.1493A>C	NP_001366580.1:p.Asn498Thr
NM_001379653.1:c.1493A>C	NP_001366582.1:p.Asn498Thr
NM_004321.8:c.1493A>C	NP_004312.2:p.Asn498Thr