Canonical Allele Identifier: CA983720090

Gene: KRT10

Linked Data

• dbSNP Id: rs1905195575
• gnomAD v3: 17-40818970-T-TGGCCGCCGCTGGAGCTTCCGCCGCCGG
• gnomAD v4: 17-40818970-T-TGGCCGCCGCTGGAGCTTCCGCCGCCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40818992_40818993insGCCGGGGCCGCCGCTGGAGCTTCCGCC , CM000679.2:g.40818992_40818993insGCCGGGGCCGCCGCTGGAGCTTCCGCC	GRCh38
NC_000017.10:g.38975244_38975245insGCCGGGGCCGCCGCTGGAGCTTCCGCC , CM000679.1:g.38975244_38975245insGCCGGGGCCGCCGCTGGAGCTTCCGCC	GRCh37
NC_000017.9:g.36228770_36228771insGCCGGGGCCGCCGCTGGAGCTTCCGCC	NCBI36
NG_008405.1:g.8641_8642insCCGGCGGCGGAAGCTCCAGCGGCGGCC
NG_033147.1:g.4901_4902insGCCGGGGCCGCCGCTGGAGCTTCCGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000269576.6:c.1564_1565insCCGGCGGCGGAAGCTCCAGCGGCGGCC MANE Select	ENSP00000269576.5:p.Gly521_His522insProGlyGlyGlySerSerSerGlyG...
ENST00000635956.2:c.1564_1565insCCGGCGGCGGAAGCTCCAGCGGCGGCC	ENSP00000490524.2:p.Gly521_His522insProGlyGlyGlySerSerSerGlyG...
ENST00000269576.5:c.1564_1565insCCGGCGGCGGAAGCTCCAGCGGCGGCC	ENSP00000269576.5:p.Gly521_His522insProGlyGlyGlySerSerSerGlyG...
NM_000421.3:c.1564_1565insCCGGCGGCGGAAGCTCCAGCGGCGGCC	NP_000412.3:p.Gly521_His522insProGlyGlyGlySerSerSerGlyGly
XM_005257343.2:c.1564_1565insCCGGCGGCGGAAGCTCCAGCGGCGGCC	XP_005257400.1:p.Gly521_His522insProGlyGlyGlySerSerSerGlyGly
XM_005257343.3:c.1564_1565insCCGGCGGCGGAAGCTCCAGCGGCGGCC	XP_005257400.1:p.Gly521_His522insProGlyGlyGlySerSerSerGlyGly
NM_000421.4:c.1564_1565insCCGGCGGCGGAAGCTCCAGCGGCGGCC	NP_000412.3:p.Gly521_His522insProGlyGlyGlySerSerSerGlyGly
NM_000421.5:c.1564_1565insCCGGCGGCGGAAGCTCCAGCGGCGGCC MANE Select	NP_000412.4:p.Gly521_His522insProGlyGlyGlySerSerSerGlyGly
NM_001379366.1:c.1564_1565insCCGGCGGCGGAAGCTCCAGCGGCGGCC	NP_001366295.1:p.Gly521_His522insProGlyGlyGlySerSerSerGlyGly