Canonical Allele Identifier: CA2618258886

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39309583-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309584dup , CM000674.2:g.39309584dup	GRCh38
NC_000012.11:g.39703386dup , CM000674.1:g.39703386dup	GRCh37
NC_000012.10:g.37989653dup	NCBI36
NG_017067.1:g.138807dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4277+2dup MANE Select	ENSP00000354878.5:n.4277+2dup
ENST00000636569.1:c.4214+2dup	ENSP00000490369.1:n.4214+2dup
ENST00000361418.9:c.4277+2dup	ENSP00000354878.5:n.4277+2dup
ENST00000361961.7:c.4238+2dup	ENSP00000354851.3:n.4238+2dup
ENST00000541463.6:c.4118+2dup	ENSP00000438075.2:n.4118+2dup
ENST00000544797.6:c.4166+2dup	ENSP00000445606.2:n.4166+2dup
ENST00000547733.1:n.1591+2dup
ENST00000551264.5:c.1220+2dup	ENSP00000448792.1:n.1220+2dup
ENST00000552961.5:c.2179+2dup
NM_001173463.1:c.4166+2dup	NP_001166934.1:n.4166+2dup
NM_001173464.1:c.4277+2dup	NP_001166935.1:n.4277+2dup
NM_001173465.1:c.4118+2dup	NP_001166936.1:n.4118+2dup
NM_017641.3:c.4238+2dup	NP_060111.2:n.4238+2dup
XM_005269007.1:c.4280+2dup	XP_005269064.1:n.4280+2dup
XM_005269008.1:c.4265+2dup	XP_005269065.1:n.4265+2dup
XM_005269009.1:c.4259+2dup	XP_005269066.1:n.4259+2dup
XM_005269010.1:c.4241+2dup	XP_005269067.1:n.4241+2dup
XM_005269011.1:c.4226+2dup	XP_005269068.1:n.4226+2dup
XM_005269012.1:c.4151+2dup	XP_005269069.1:n.4151+2dup
XM_005269013.1:c.4136+2dup	XP_005269070.1:n.4136+2dup
XM_005269014.1:c.4097+2dup	XP_005269071.1:n.4097+2dup
XM_006719493.1:c.4220+2dup	XP_006719556.1:n.4220+2dup
XM_006719494.1:c.4148+2dup	XP_006719557.1:n.4148+2dup
XM_006719496.1:c.4205+2dup	XP_006719559.1:n.4205+2dup
XM_011538556.1:c.4211+2dup	XP_011536858.1:n.4211+2dup
XM_005269007.3:c.4280+2dup	XP_005269064.1:n.4280+2dup
XM_005269008.3:c.4265+2dup	XP_005269065.1:n.4265+2dup
XM_005269009.3:c.4259+2dup	XP_005269066.1:n.4259+2dup
XM_005269010.3:c.4241+2dup	XP_005269067.1:n.4241+2dup
XM_005269011.3:c.4226+2dup	XP_005269068.1:n.4226+2dup
XM_005269012.3:c.4151+2dup	XP_005269069.1:n.4151+2dup
XM_005269013.3:c.4136+2dup	XP_005269070.1:n.4136+2dup
XM_005269014.3:c.4097+2dup	XP_005269071.1:n.4097+2dup
XM_006719493.3:c.4220+2dup	XP_006719556.1:n.4220+2dup
XM_006719494.3:c.4148+2dup	XP_006719557.1:n.4148+2dup
XM_011538556.3:c.4211+2dup	XP_011536858.1:n.4211+2dup
XM_017019607.2:c.4226+2dup	XP_016875096.1:n.4226+2dup
XM_017019608.2:c.4187+2dup	XP_016875097.1:n.4187+2dup
XM_017019609.2:c.4076+2dup	XP_016875098.1:n.4076+2dup
XM_017019610.2:c.4076+2dup	XP_016875099.1:n.4076+2dup
XM_017019611.2:c.4058+2dup	XP_016875100.1:n.4058+2dup
NM_001173463.2:c.4166+2dup	NP_001166934.1:n.4166+2dup
NM_001173464.2:c.4277+2dup MANE Select	NP_001166935.1:n.4277+2dup
NM_001173465.2:c.4118+2dup	NP_001166936.1:n.4118+2dup
NM_017641.4:c.4238+2dup	NP_060111.2:n.4238+2dup
NM_001378439.1:c.4280+2dup	NP_001365368.1:n.4280+2dup
NM_001378440.1:c.4265+2dup	NP_001365369.1:n.4265+2dup
NM_001378441.1:c.4241+2dup	NP_001365370.1:n.4241+2dup