Canonical Allele Identifier: CA384923466
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52910442A>C (hg19) chr12:g.52516658A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516658A>C , CM000674.2:g.52516658A>C GRCh38
NC_000012.11:g.52910442A>C , CM000674.1:g.52910442A>C GRCh37
NC_000012.10:g.51196709A>C NCBI36
NG_008297.1:g.8802T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1418T>G MANE Select ENSP00000252242.4:p.Leu473Arg
ENST00000252242.8:c.1418T>G ENSP00000252242.4:p.Leu473Arg
ENST00000548409.5:c.540T>G
ENST00000549511.5:n.625T>G
ENST00000552629.5:n.1516T>G
NM_000424.3:c.1418T>G NP_000415.2:p.Leu473Arg
NM_000424.4:c.1418T>G MANE Select NP_000415.2:p.Leu473Arg
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Search 100 bp 3'