Canonical Allele Identifier: CA2726183848
Gene: KRT2 HGNC NCBI

Linked Data

dbSNP Id: rs2120956273
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651857_52651858insGCCGCTCCCGCCTCCAAA , CM000674.2:g.52651857_52651858insGCCGCTCCCGCCTCCAAA GRCh38
NC_000012.11:g.53045641_53045642insGCCGCTCCCGCCTCCAAA , CM000674.1:g.53045641_53045642insGCCGCTCCCGCCTCCAAA GRCh37
NC_000012.10:g.51331908_51331909insGCCGCTCCCGCCTCCAAA NCBI36
NG_008296.1:g.5329_5330insGAGCGGCTTTGGAGGCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.296_297insGAGCGGCTTTGGAGGCGG MANE Select ENSP00000310861.3:p.Gly99_Ser100insSerGlyPheGlyGlyGly
ENST00000309680.3:c.296_297insGAGCGGCTTTGGAGGCGG ENSP00000310861.3:p.Gly99_Ser100insSerGlyPheGlyGlyGly
NM_000423.2:c.296_297insGAGCGGCTTTGGAGGCGG NP_000414.2:p.Gly99_Ser100insSerGlyPheGlyGlyGly
NM_000423.3:c.296_297insGAGCGGCTTTGGAGGCGG MANE Select NP_000414.2:p.Gly99_Ser100insSerGlyPheGlyGlyGly
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