Canonical Allele Identifier: CA384923944
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52910532T>A (hg19) chr12:g.52516748T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516748T>A , CM000674.2:g.52516748T>A GRCh38
NC_000012.11:g.52910532T>A , CM000674.1:g.52910532T>A GRCh37
NC_000012.10:g.51196799T>A NCBI36
NG_008297.1:g.8712A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1328A>T MANE Select ENSP00000252242.4:p.Lys443Met
ENST00000252242.8:c.1328A>T ENSP00000252242.4:p.Lys443Met
ENST00000547890.5:n.706A>T
ENST00000548409.5:c.450A>T
ENST00000549511.5:n.535A>T
ENST00000552629.5:n.1426A>T
NM_000424.3:c.1328A>T NP_000415.2:p.Lys443Met
NM_000424.4:c.1328A>T MANE Select NP_000415.2:p.Lys443Met
Search 100 bp 5'
Search 100 bp 3'