Canonical Allele Identifier: CA2036538948
Gene: KRT5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516710_52516714delinsGCTCC , CM000674.2:g.52516710_52516714delinsGCTCC GRCh38
NC_000012.11:g.52910494_52910498delinsGCTCC , CM000674.1:g.52910494_52910498delinsGCTCC GRCh37
NC_000012.10:g.51196761_51196765delinsGCTCC NCBI36
NG_008297.1:g.8746_8750delinsGGAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1362_1366delinsGGAGC MANE Select ENSP00000252242.4:p.Gln454=
ENST00000252242.8:c.1362_1366delinsGGAGC ENSP00000252242.4:p.Gln454=
ENST00000547890.5:n.740_744delinsGGAGC
ENST00000548409.5:c.484_488delinsGGAGC
ENST00000549511.5:n.569_573delinsGGAGC
ENST00000552629.5:n.1460_1464delinsGGAGC
NM_000424.3:c.1362_1366delinsGGAGC NP_000415.2:p.Gln454=
NM_000424.4:c.1362_1366delinsGGAGC MANE Select NP_000415.2:p.Gln454=
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