Canonical Allele Identifier: CA384387196

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703463A>G (hg19) ; chr12:g.39309661A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309661A>G , CM000674.2:g.39309661A>G	GRCh38
NC_000012.11:g.39703463A>G , CM000674.1:g.39703463A>G	GRCh37
NC_000012.10:g.37989730A>G	NCBI36
NG_017067.1:g.138730T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4202T>C MANE Select	ENSP00000354878.5:p.Leu1401Ser
ENST00000636569.1:c.4139T>C	ENSP00000490369.1:p.Leu1380Ser
ENST00000361418.9:c.4202T>C	ENSP00000354878.5:p.Leu1401Ser
ENST00000361961.7:c.4163T>C	ENSP00000354851.3:p.Leu1388Ser
ENST00000541463.6:c.4043T>C	ENSP00000438075.2:p.Leu1348Ser
ENST00000544797.6:c.4091T>C	ENSP00000445606.2:p.Leu1364Ser
ENST00000547733.1:n.1516T>C
ENST00000551264.5:c.1145T>C	ENSP00000448792.1:p.Leu382Ser
ENST00000552961.5:c.2104T>C
NM_001173463.1:c.4091T>C	NP_001166934.1:p.Leu1364Ser
NM_001173464.1:c.4202T>C	NP_001166935.1:p.Leu1401Ser
NM_001173465.1:c.4043T>C	NP_001166936.1:p.Leu1348Ser
NM_017641.3:c.4163T>C	NP_060111.2:p.Leu1388Ser
XM_005269007.1:c.4205T>C	XP_005269064.1:p.Leu1402Ser
XM_005269008.1:c.4190T>C	XP_005269065.1:p.Leu1397Ser
XM_005269009.1:c.4184T>C	XP_005269066.1:p.Leu1395Ser
XM_005269010.1:c.4166T>C	XP_005269067.1:p.Leu1389Ser
XM_005269011.1:c.4151T>C	XP_005269068.1:p.Leu1384Ser
XM_005269012.1:c.4076T>C	XP_005269069.1:p.Leu1359Ser
XM_005269013.1:c.4061T>C	XP_005269070.1:p.Leu1354Ser
XM_005269014.1:c.4022T>C	XP_005269071.1:p.Leu1341Ser
XM_006719493.1:c.4145T>C	XP_006719556.1:p.Leu1382Ser
XM_006719494.1:c.4073T>C	XP_006719557.1:p.Leu1358Ser
XM_006719496.1:c.4130T>C	XP_006719559.1:p.Leu1377Ser
XM_011538556.1:c.4136T>C	XP_011536858.1:p.Leu1379Ser
XM_005269007.3:c.4205T>C	XP_005269064.1:p.Leu1402Ser
XM_005269008.3:c.4190T>C	XP_005269065.1:p.Leu1397Ser
XM_005269009.3:c.4184T>C	XP_005269066.1:p.Leu1395Ser
XM_005269010.3:c.4166T>C	XP_005269067.1:p.Leu1389Ser
XM_005269011.3:c.4151T>C	XP_005269068.1:p.Leu1384Ser
XM_005269012.3:c.4076T>C	XP_005269069.1:p.Leu1359Ser
XM_005269013.3:c.4061T>C	XP_005269070.1:p.Leu1354Ser
XM_005269014.3:c.4022T>C	XP_005269071.1:p.Leu1341Ser
XM_006719493.3:c.4145T>C	XP_006719556.1:p.Leu1382Ser
XM_006719494.3:c.4073T>C	XP_006719557.1:p.Leu1358Ser
XM_011538556.3:c.4136T>C	XP_011536858.1:p.Leu1379Ser
XM_017019607.2:c.4151T>C	XP_016875096.1:p.Leu1384Ser
XM_017019608.2:c.4112T>C	XP_016875097.1:p.Leu1371Ser
XM_017019609.2:c.4001T>C	XP_016875098.1:p.Leu1334Ser
XM_017019610.2:c.4001T>C	XP_016875099.1:p.Leu1334Ser
XM_017019611.2:c.3983T>C	XP_016875100.1:p.Leu1328Ser
NM_001173463.2:c.4091T>C	NP_001166934.1:p.Leu1364Ser
NM_001173464.2:c.4202T>C MANE Select	NP_001166935.1:p.Leu1401Ser
NM_001173465.2:c.4043T>C	NP_001166936.1:p.Leu1348Ser
NM_017641.4:c.4163T>C	NP_060111.2:p.Leu1388Ser
NM_001378439.1:c.4205T>C	NP_001365368.1:p.Leu1402Ser
NM_001378440.1:c.4190T>C	NP_001365369.1:p.Leu1397Ser
NM_001378441.1:c.4166T>C	NP_001365370.1:p.Leu1389Ser