Canonical Allele Identifier: CA658798830
Gene: KRT10 HGNC NCBI

Linked Data

ClinVar Variation Id: 509767
ClinVar RCV Id: RCV000606079
dbSNP Id: rs753095095

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40819087_40819116dup , CM000679.2:g.40819087_40819116dup GRCh38
NC_000017.10:g.38975339_38975368dup , CM000679.1:g.38975339_38975368dup GRCh37
NC_000017.9:g.36228865_36228894dup NCBI36
NG_008405.1:g.8505_8534dup
NG_033147.1:g.4996_5025dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000269576.6:c.1428_1457dup MANE Select ENSP00000269576.5:p.Gly486_His487insSerSerGlyGlyGlySerSerGlyG...
ENST00000635956.2:c.1428_1457dup ENSP00000490524.2:p.Gly486_His487insSerSerGlyGlyGlySerSerGlyG...
ENST00000269576.5:c.1428_1457dup ENSP00000269576.5:p.Gly486_His487insSerSerGlyGlyGlySerSerGlyG...
NM_000421.3:c.1428_1457dup NP_000412.3:p.Gly486_His487insSerSerGlyGlyGlySerSerGlyGlyGly
XM_005257343.2:c.1428_1457dup XP_005257400.1:p.Gly486_His487insSerSerGlyGlyGlySerSerGlyGlyG...
XM_005257343.3:c.1428_1457dup XP_005257400.1:p.Gly486_His487insSerSerGlyGlyGlySerSerGlyGlyG...
NM_000421.4:c.1428_1457dup NP_000412.3:p.Gly486_His487insSerSerGlyGlyGlySerSerGlyGlyGly
NM_000421.5:c.1428_1457dup MANE Select NP_000412.4:p.Gly486_His487insSerSerGlyGlyGlySerSerGlyGlyGly
NM_001379366.1:c.1428_1457dup NP_001366295.1:p.Gly486_His487insSerSerGlyGlyGlySerSerGlyGlyG...