Canonical Allele Identifier: CA10642044

Gene: KIF21A

Linked Data

• ClinVar Variation Id: 308530
• ClinVar RCV Id: RCV000291274
• dbSNP Id: rs886049334
• gnomAD v3: 12-39293578-T-TA
• gnomAD v4: 12-39293578-T-TA
• MyVariant Identifiers: chr12:g.39687381dupA (hg19) ; chr12:g.39687380_39687381insA (hg19) ; chr12:g.39293579dupA (hg38) ; chr12:g.39293578_39293579insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39293584dup , CM000674.2:g.39293584dup	GRCh38
NC_000012.11:g.39687386dup , CM000674.1:g.39687386dup	GRCh37
NC_000012.10:g.37973653dup	NCBI36
NG_017067.1:g.154812dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.*845dup MANE Select	ENSP00000354878.5:n.*845dup
ENST00000636569.1:c.5807dup	ENSP00000490369.1:n.5807dup
ENST00000361961.7:c.*845dup	ENSP00000354851.3:n.*845dup
ENST00000547733.1:n.3184dup
ENST00000551264.5:c.2813dup	ENSP00000448792.1:n.2813dup
ENST00000552961.5:c.3772dup
NM_001173463.1:c.*845dup	NP_001166934.1:n.*845dup
NM_001173464.1:c.*845dup	NP_001166935.1:n.*845dup
NM_001173465.1:c.*845dup	NP_001166936.1:n.*845dup
NM_017641.3:c.*845dup	NP_060111.2:n.*845dup
XM_005269007.1:c.*845dup	XP_005269064.1:n.*845dup
XM_005269008.1:c.*845dup	XP_005269065.1:n.*845dup
XM_005269009.1:c.*845dup	XP_005269066.1:n.*845dup
XM_005269010.1:c.*845dup	XP_005269067.1:n.*845dup
XM_005269011.1:c.*845dup	XP_005269068.1:n.*845dup
XM_005269012.1:c.*845dup	XP_005269069.1:n.*845dup
XM_005269013.1:c.*845dup	XP_005269070.1:n.*845dup
XM_005269014.1:c.*845dup	XP_005269071.1:n.*845dup
XM_006719493.1:c.*845dup	XP_006719556.1:n.*845dup
XM_006719494.1:c.*845dup	XP_006719557.1:n.*845dup
XM_006719496.1:c.*845dup	XP_006719559.1:n.*845dup
XM_011538556.1:c.*845dup	XP_011536858.1:n.*845dup
XM_005269007.3:c.*845dup	XP_005269064.1:n.*845dup
XM_005269008.3:c.*845dup	XP_005269065.1:n.*845dup
XM_005269009.3:c.*845dup	XP_005269066.1:n.*845dup
XM_005269010.3:c.*845dup	XP_005269067.1:n.*845dup
XM_005269011.3:c.*845dup	XP_005269068.1:n.*845dup
XM_005269012.3:c.*845dup	XP_005269069.1:n.*845dup
XM_005269013.3:c.*845dup	XP_005269070.1:n.*845dup
XM_005269014.3:c.*845dup	XP_005269071.1:n.*845dup
XM_006719493.3:c.*845dup	XP_006719556.1:n.*845dup
XM_006719494.3:c.*845dup	XP_006719557.1:n.*845dup
XM_011538556.3:c.*845dup	XP_011536858.1:n.*845dup
XM_017019607.2:c.*845dup	XP_016875096.1:n.*845dup
XM_017019608.2:c.*845dup	XP_016875097.1:n.*845dup
XM_017019609.2:c.*845dup	XP_016875098.1:n.*845dup
XM_017019610.2:c.*845dup	XP_016875099.1:n.*845dup
XM_017019611.2:c.*845dup	XP_016875100.1:n.*845dup
NM_001173463.2:c.*845dup	NP_001166934.1:n.*845dup
NM_001173464.2:c.*845dup MANE Select	NP_001166935.1:n.*845dup
NM_001173465.2:c.*845dup	NP_001166936.1:n.*845dup
NM_017641.4:c.*845dup	NP_060111.2:n.*845dup
NM_001378439.1:c.*845dup	NP_001365368.1:n.*845dup
NM_001378440.1:c.*845dup	NP_001365369.1:n.*845dup
NM_001378441.1:c.*845dup	NP_001365370.1:n.*845dup