Canonical Allele Identifier: CA2618946315
Gene: KRT2 HGNC NCBI

Linked Data

gnomAD v4: 12-52651824-C-CGCTGCCACCTCCAAAGCT
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651831_52651848dup , CM000674.2:g.52651831_52651848dup GRCh38
NC_000012.11:g.53045615_53045632dup , CM000674.1:g.53045615_53045632dup GRCh37
NC_000012.10:g.51331882_51331899dup NCBI36
NG_008296.1:g.5334_5351dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.301_318dup MANE Select ENSP00000310861.3:p.Ser106_Gly107insSerPheGlyGlyGlySer
ENST00000309680.3:c.301_318dup ENSP00000310861.3:p.Ser106_Gly107insSerPheGlyGlyGlySer
NM_000423.2:c.301_318dup NP_000414.2:p.Ser106_Gly107insSerPheGlyGlyGlySer
NM_000423.3:c.301_318dup MANE Select NP_000414.2:p.Ser106_Gly107insSerPheGlyGlyGlySer
Search 100 bp 5'
Search 100 bp 3'