Canonical Allele Identifier: CA2036540504
Gene: KRT5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519892G= , CM000674.2:g.52519892G= GRCh38
NC_000012.11:g.52913676G= , CM000674.1:g.52913676G= GRCh37
NC_000012.10:g.51199943G= NCBI36
NG_008297.1:g.5568C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.405C= MANE Select ENSP00000252242.4:p.Cys135=
ENST00000252242.8:c.405C= ENSP00000252242.4:p.Cys135=
ENST00000549420.1:c.75C= ENSP00000447209.1:p.Cys25=
ENST00000551275.1:c.300C= ENSP00000448041.1:p.Cys100=
ENST00000552629.5:n.503C=
NM_000424.3:c.405C= NP_000415.2:p.Cys135=
NM_000424.4:c.405C= MANE Select NP_000415.2:p.Cys135=
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