Canonical Allele Identifier: CA626212448

Gene: KRT10

Linked Data

• dbSNP Id: rs1398858290
• gnomAD v2: 17-38975218-G-GCCGTGGCCGCCGCTGGAGCTTCCGCCC
• gnomAD v3: 17-40818966-G-GCCGTGGCCGCCGCTGGAGCTTCCGCCC
• gnomAD v4: 17-40818966-G-GCCGTGGCCGCCGCTGGAGCTTCCGCCC
• MyVariant Identifiers: chr17:g.38975218_38975219insCCGTGGCCGCCGCTGGAGCTTCCGCCC (hg19) ; chr17:g.40818966_40818967insCCGTGGCCGCCGCTGGAGCTTCCGCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40818971_40818997dup , CM000679.2:g.40818971_40818997dup	GRCh38
NC_000017.10:g.38975223_38975249dup , CM000679.1:g.38975223_38975249dup	GRCh37
NC_000017.9:g.36228749_36228775dup	NCBI36
NG_008405.1:g.8619_8645dup
NG_033147.1:g.4880_4906dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000269576.6:c.1542_1568dup MANE Select	ENSP00000269576.5:p.Gly523_Gly524insGlyGlySerSerSerGlyGlyHisG...
ENST00000635956.2:c.1542_1568dup	ENSP00000490524.2:p.Gly523_Gly524insGlyGlySerSerSerGlyGlyHisG...
ENST00000269576.5:c.1542_1568dup	ENSP00000269576.5:p.Gly523_Gly524insGlyGlySerSerSerGlyGlyHisG...
NM_000421.3:c.1542_1568dup	NP_000412.3:p.Gly523_Gly524insGlyGlySerSerSerGlyGlyHisGly
XM_005257343.2:c.1542_1568dup	XP_005257400.1:p.Gly523_Gly524insGlyGlySerSerSerGlyGlyHisGly
XM_005257343.3:c.1542_1568dup	XP_005257400.1:p.Gly523_Gly524insGlyGlySerSerSerGlyGlyHisGly
NM_000421.4:c.1542_1568dup	NP_000412.3:p.Gly523_Gly524insGlyGlySerSerSerGlyGlyHisGly
NM_000421.5:c.1542_1568dup MANE Select	NP_000412.4:p.Gly523_Gly524insGlyGlySerSerSerGlyGlyHisGly
NM_001379366.1:c.1542_1568dup	NP_001366295.1:p.Gly523_Gly524insGlyGlySerSerSerGlyGlyHisGly