Canonical Allele Identifier: CA2036540421
Gene: KRT5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519747_52519750delinsCGAT , CM000674.2:g.52519747_52519750delinsCGAT GRCh38
NC_000012.11:g.52913531_52913534delinsCGAT , CM000674.1:g.52913531_52913534delinsCGAT GRCh37
NC_000012.10:g.51199798_51199801delinsCGAT NCBI36
NG_008297.1:g.5710_5713delinsATCG

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.547_550delinsATCG MANE Select ENSP00000252242.4:p.Ile183=
ENST00000252242.8:c.547_550delinsATCG ENSP00000252242.4:p.Ile183=
ENST00000549420.1:c.217_220delinsATCG ENSP00000447209.1:p.Ile73=
ENST00000552629.5:n.645_648delinsATCG
NM_000424.3:c.547_550delinsATCG NP_000415.2:p.Ile183=
NM_000424.4:c.547_550delinsATCG MANE Select NP_000415.2:p.Ile183=
Search 100 bp 5'
Search 100 bp 3'