Canonical Allele Identifier: CA983720051

Gene: KRT10

Linked Data

• ClinVar Variation Id: 2987077
• ClinVar RCV Id: RCV003848716
• dbSNP Id: rs1555548442
• gnomAD v3: 17-40818962-T-TGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCGCCGTGGCCGCCGCTGGAGCTTCC
• gnomAD v4: 17-40818962-T-TGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCGCCGTGGCCGCCGCTGGAGCTTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40818992_40818993insGCCGTGGCCGCCGCTGGAGCTTCCGCCGCCGTGGCCGCCGCTGGAGCTTCCGCC , CM000679.2:g.40818992_40818993insGCCGTGGCCGCCGCTGGAGCTTCCGCCGCCGTGGCCGCCGCTGGAGCTTCCGCC	GRCh38
NC_000017.10:g.38975244_38975245insGCCGTGGCCGCCGCTGGAGCTTCCGCCGCCGTGGCCGCCGCTGGAGCTTCCGCC , CM000679.1:g.38975244_38975245insGCCGTGGCCGCCGCTGGAGCTTCCGCCGCCGTGGCCGCCGCTGGAGCTTCCGCC	GRCh37
NC_000017.9:g.36228770_36228771insGCCGTGGCCGCCGCTGGAGCTTCCGCCGCCGTGGCCGCCGCTGGAGCTTCCGCC	NCBI36
NG_008405.1:g.8649_8650insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC
NG_033147.1:g.4901_4902insGCCGTGGCCGCCGCTGGAGCTTCCGCCGCCGTGGCCGCCGCTGGAGCTTCCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269576.6:c.1572_1573insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC MANE Select	ENSP00000269576.5:p.Gly524_Ser525insGlySerSerSerGlyGlyHisGlyG...
ENST00000635956.2:c.1572_1573insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC	ENSP00000490524.2:p.Gly524_Ser525insGlySerSerSerGlyGlyHisGlyG...
ENST00000269576.5:c.1572_1573insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC	ENSP00000269576.5:p.Gly524_Ser525insGlySerSerSerGlyGlyHisGlyG...
NM_000421.3:c.1572_1573insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC	NP_000412.3:p.Gly524_Ser525insGlySerSerSerGlyGlyHisGlyGlyGlyS...
XM_005257343.2:c.1572_1573insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC	XP_005257400.1:p.Gly524_Ser525insGlySerSerSerGlyGlyHisGlyGlyG...
XM_005257343.3:c.1572_1573insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC	XP_005257400.1:p.Gly524_Ser525insGlySerSerSerGlyGlyHisGlyGlyG...
NM_000421.4:c.1572_1573insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC	NP_000412.3:p.Gly524_Ser525insGlySerSerSerGlyGlyHisGlyGlyGlyS...
NM_000421.5:c.1572_1573insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC MANE Select	NP_000412.4:p.Gly524_Ser525insGlySerSerSerGlyGlyHisGlyGlyGlyS...
NM_001379366.1:c.1572_1573insGGAAGCTCCAGCGGCGGCCACGGCGGCGGAAGCTCCAGCGGCGGCCACGGCGGC	NP_001366295.1:p.Gly524_Ser525insGlySerSerSerGlyGlyHisGlyGlyG...