Canonical Allele Identifier: CA384923457
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52910439A>T (hg19) chr12:g.52516655A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516655A>T , CM000674.2:g.52516655A>T GRCh38
NC_000012.11:g.52910439A>T , CM000674.1:g.52910439A>T GRCh37
NC_000012.10:g.51196706A>T NCBI36
NG_008297.1:g.8805T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.1421T>A MANE Select ENSP00000252242.4:p.Leu474Gln
ENST00000252242.8:c.1421T>A ENSP00000252242.4:p.Leu474Gln
ENST00000548409.5:c.543T>A
ENST00000549511.5:n.628T>A
ENST00000552629.5:n.1519T>A
NM_000424.3:c.1421T>A NP_000415.2:p.Leu474Gln
NM_000424.4:c.1421T>A MANE Select NP_000415.2:p.Leu474Gln
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