Canonical Allele Identifier: CA2030528386

Gene: KIF21A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39332656T= , CM000674.2:g.39332656T=	GRCh38
NC_000012.11:g.39726458T= , CM000674.1:g.39726458T=	GRCh37
NC_000012.10:g.38012725T=	NCBI36
NG_017067.1:g.115735A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.2791A= MANE Select	ENSP00000354878.5:p.Thr931=
ENST00000636569.1:c.2725A=	ENSP00000490369.1:p.Thr909=
ENST00000361418.9:c.2791A=	ENSP00000354878.5:p.Thr931=
ENST00000361961.7:c.2752A=	ENSP00000354851.3:p.Thr918=
ENST00000541463.6:c.2683A=	ENSP00000438075.2:p.Thr895=
ENST00000544797.6:c.2752A=	ENSP00000445606.2:p.Thr918=
ENST00000547108.5:c.564A=
ENST00000552961.5:c.834A=
NM_001173463.1:c.2752A=	NP_001166934.1:p.Thr918=
NM_001173464.1:c.2791A=	NP_001166935.1:p.Thr931=
NM_001173465.1:c.2683A=	NP_001166936.1:p.Thr895=
NM_017641.3:c.2752A=	NP_060111.2:p.Thr918=
XM_005269007.1:c.2791A=	XP_005269064.1:p.Thr931=
XM_005269008.1:c.2791A=	XP_005269065.1:p.Thr931=
XM_005269009.1:c.2791A=	XP_005269066.1:p.Thr931=
XM_005269010.1:c.2752A=	XP_005269067.1:p.Thr918=
XM_005269011.1:c.2791A=	XP_005269068.1:p.Thr931=
XM_005269012.1:c.2791A=	XP_005269069.1:p.Thr931=
XM_005269013.1:c.2791A=	XP_005269070.1:p.Thr931=
XM_005269014.1:c.2791A=	XP_005269071.1:p.Thr931=
XM_006719493.1:c.2752A=	XP_006719556.1:p.Thr918=
XM_006719494.1:c.2791A=	XP_006719557.1:p.Thr931=
XM_006719496.1:c.2752A=	XP_006719559.1:p.Thr918=
XM_011538556.1:c.2722A=	XP_011536858.1:p.Thr908=
XR_429108.1:n.3123A=
XM_005269007.3:c.2791A=	XP_005269064.1:p.Thr931=
XM_005269008.3:c.2791A=	XP_005269065.1:p.Thr931=
XM_005269009.3:c.2791A=	XP_005269066.1:p.Thr931=
XM_005269010.3:c.2752A=	XP_005269067.1:p.Thr918=
XM_005269011.3:c.2791A=	XP_005269068.1:p.Thr931=
XM_005269012.3:c.2791A=	XP_005269069.1:p.Thr931=
XM_005269013.3:c.2791A=	XP_005269070.1:p.Thr931=
XM_005269014.3:c.2791A=	XP_005269071.1:p.Thr931=
XM_006719493.3:c.2752A=	XP_006719556.1:p.Thr918=
XM_006719494.3:c.2791A=	XP_006719557.1:p.Thr931=
XM_011538556.3:c.2722A=	XP_011536858.1:p.Thr908=
XM_017019607.2:c.2752A=	XP_016875096.1:p.Thr918=
XM_017019608.2:c.2752A=	XP_016875097.1:p.Thr918=
XM_017019609.2:c.2752A=	XP_016875098.1:p.Thr918=
XM_017019610.2:c.2791A=	XP_016875099.1:p.Thr931=
XM_017019611.2:c.2752A=	XP_016875100.1:p.Thr918=
NM_001173463.2:c.2752A=	NP_001166934.1:p.Thr918=
NM_001173464.2:c.2791A= MANE Select	NP_001166935.1:p.Thr931=
NM_001173465.2:c.2683A=	NP_001166936.1:p.Thr895=
NM_017641.4:c.2752A=	NP_060111.2:p.Thr918=
NM_001378439.1:c.2791A=	NP_001365368.1:p.Thr931=
NM_001378440.1:c.2791A=	NP_001365369.1:p.Thr931=
NM_001378441.1:c.2752A=	NP_001365370.1:p.Thr918=