Canonical Allele Identifier: CA2618261893

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39332510-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39332510_39332511insC , CM000674.2:g.39332510_39332511insC	GRCh38
NC_000012.11:g.39726312_39726313insC , CM000674.1:g.39726312_39726313insC	GRCh37
NC_000012.10:g.38012579_38012580insC	NCBI36
NG_017067.1:g.115880_115881insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.2856+80_2856+81insG MANE Select	ENSP00000354878.5:n.2856+80_2856+81insG
ENST00000636569.1:c.2790+80_2790+81insG	ENSP00000490369.1:n.2790+80_2790+81insG
ENST00000361418.9:c.2856+80_2856+81insG	ENSP00000354878.5:n.2856+80_2856+81insG
ENST00000361961.7:c.2817+80_2817+81insG	ENSP00000354851.3:n.2817+80_2817+81insG
ENST00000541463.6:c.2748+80_2748+81insG	ENSP00000438075.2:n.2748+80_2748+81insG
ENST00000544797.6:c.2817+80_2817+81insG	ENSP00000445606.2:n.2817+80_2817+81insG
ENST00000547108.5:c.629+80_629+81insG
ENST00000552961.5:c.899+80_899+81insG
NM_001173463.1:c.2817+80_2817+81insG	NP_001166934.1:n.2817+80_2817+81insG
NM_001173464.1:c.2856+80_2856+81insG	NP_001166935.1:n.2856+80_2856+81insG
NM_001173465.1:c.2748+80_2748+81insG	NP_001166936.1:n.2748+80_2748+81insG
NM_017641.3:c.2817+80_2817+81insG	NP_060111.2:n.2817+80_2817+81insG
XM_005269007.1:c.2856+80_2856+81insG	XP_005269064.1:n.2856+80_2856+81insG
XM_005269008.1:c.2856+80_2856+81insG	XP_005269065.1:n.2856+80_2856+81insG
XM_005269009.1:c.2856+80_2856+81insG	XP_005269066.1:n.2856+80_2856+81insG
XM_005269010.1:c.2817+80_2817+81insG	XP_005269067.1:n.2817+80_2817+81insG
XM_005269011.1:c.2856+80_2856+81insG	XP_005269068.1:n.2856+80_2856+81insG
XM_005269012.1:c.2856+80_2856+81insG	XP_005269069.1:n.2856+80_2856+81insG
XM_005269013.1:c.2856+80_2856+81insG	XP_005269070.1:n.2856+80_2856+81insG
XM_005269014.1:c.2856+80_2856+81insG	XP_005269071.1:n.2856+80_2856+81insG
XM_006719493.1:c.2817+80_2817+81insG	XP_006719556.1:n.2817+80_2817+81insG
XM_006719494.1:c.2856+80_2856+81insG	XP_006719557.1:n.2856+80_2856+81insG
XM_006719496.1:c.2817+80_2817+81insG	XP_006719559.1:n.2817+80_2817+81insG
XM_011538556.1:c.2787+80_2787+81insG	XP_011536858.1:n.2787+80_2787+81insG
XR_429108.1:n.3188+80_3188+81insG
XM_005269007.3:c.2856+80_2856+81insG	XP_005269064.1:n.2856+80_2856+81insG
XM_005269008.3:c.2856+80_2856+81insG	XP_005269065.1:n.2856+80_2856+81insG
XM_005269009.3:c.2856+80_2856+81insG	XP_005269066.1:n.2856+80_2856+81insG
XM_005269010.3:c.2817+80_2817+81insG	XP_005269067.1:n.2817+80_2817+81insG
XM_005269011.3:c.2856+80_2856+81insG	XP_005269068.1:n.2856+80_2856+81insG
XM_005269012.3:c.2856+80_2856+81insG	XP_005269069.1:n.2856+80_2856+81insG
XM_005269013.3:c.2856+80_2856+81insG	XP_005269070.1:n.2856+80_2856+81insG
XM_005269014.3:c.2856+80_2856+81insG	XP_005269071.1:n.2856+80_2856+81insG
XM_006719493.3:c.2817+80_2817+81insG	XP_006719556.1:n.2817+80_2817+81insG
XM_006719494.3:c.2856+80_2856+81insG	XP_006719557.1:n.2856+80_2856+81insG
XM_011538556.3:c.2787+80_2787+81insG	XP_011536858.1:n.2787+80_2787+81insG
XM_017019607.2:c.2817+80_2817+81insG	XP_016875096.1:n.2817+80_2817+81insG
XM_017019608.2:c.2817+80_2817+81insG	XP_016875097.1:n.2817+80_2817+81insG
XM_017019609.2:c.2817+80_2817+81insG	XP_016875098.1:n.2817+80_2817+81insG
XM_017019610.2:c.2856+80_2856+81insG	XP_016875099.1:n.2856+80_2856+81insG
XM_017019611.2:c.2817+80_2817+81insG	XP_016875100.1:n.2817+80_2817+81insG
NM_001173463.2:c.2817+80_2817+81insG	NP_001166934.1:n.2817+80_2817+81insG
NM_001173464.2:c.2856+80_2856+81insG MANE Select	NP_001166935.1:n.2856+80_2856+81insG
NM_001173465.2:c.2748+80_2748+81insG	NP_001166936.1:n.2748+80_2748+81insG
NM_017641.4:c.2817+80_2817+81insG	NP_060111.2:n.2817+80_2817+81insG
NM_001378439.1:c.2856+80_2856+81insG	NP_001365368.1:n.2856+80_2856+81insG
NM_001378440.1:c.2856+80_2856+81insG	NP_001365369.1:n.2856+80_2856+81insG
NM_001378441.1:c.2817+80_2817+81insG	NP_001365370.1:n.2817+80_2817+81insG