Canonical Allele Identifier: CA658798829
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 510707
ClinVar RCV Id: RCV000609132
dbSNP Id: rs1555548541
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819076_40819092delinsAG , CM000679.2:g.40819076_40819092delinsAG GRCh38
NC_000017.10:g.38975328_38975344delinsAG , CM000679.1:g.38975328_38975344delinsAG GRCh37
NC_000017.9:g.36228854_36228870delinsAG NCBI36
NG_008405.1:g.8520_8536delinsCT
NG_033147.1:g.4985_5001delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1443_1459delinsCT MANE Select ENSP00000269576.5:p.Ser482_His487delinsTyr
ENST00000635956.2:c.1443_1459delinsCT ENSP00000490524.2:p.Ser482_His487delinsTyr
ENST00000269576.5:c.1443_1459delinsCT ENSP00000269576.5:p.Ser482_His487delinsTyr
NM_000421.3:c.1443_1459delinsCT NP_000412.3:p.Ser482_His487delinsTyr
XM_005257343.2:c.1443_1459delinsCT XP_005257400.1:p.Ser482_His487delinsTyr
XM_005257343.3:c.1443_1459delinsCT XP_005257400.1:p.Ser482_His487delinsTyr
NM_000421.4:c.1443_1459delinsCT NP_000412.3:p.Ser482_His487delinsTyr
NM_000421.5:c.1443_1459delinsCT MANE Select NP_000412.4:p.Ser482_His487delinsTyr
NM_001379366.1:c.1443_1459delinsCT NP_001366295.1:p.Ser482_His487delinsTyr
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