Allele Registry

Canonical Allele Identifier: CA16042806

Gene: KIF11 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr10:g.92616744dupT

GRCh37 chr10:g.94376501dupT

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000413281

ClinVar Variation:

373017

dbSNP:

1057518144

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.92616744dup , CM000672.2:g.92616744dup	GRCh38
NC_000010.10:g.94376501dup , CM000672.1:g.94376501dup	GRCh37
NC_000010.9:g.94366481dup	NCBI36
NG_032580.1:g.28677dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260731.5:c.1040dup MANE Select	ENSP00000260731.3:p.Ser348GlufsTer8
ENST00000676621.1:c.1040dup	ENSP00000503639.1:p.Ser348GlufsTer8
ENST00000676647.1:c.833dup	ENSP00000503394.1:p.Ser279GlufsTer8
ENST00000676757.1:c.833dup	ENSP00000504289.1:p.Ser279GlufsTer8
ENST00000677720.1:c.1040dup	ENSP00000504840.1:p.Ser348GlufsTer8
ENST00000260731.4:c.1040dup	ENSP00000260731.3:p.Ser348GlufsTer8
NM_004523.3:c.1040dup	NP_004514.2:p.Ser348GlufsTer8
NM_004523.4:c.1040dup MANE Select	NP_004514.2:p.Ser348GlufsTer8

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