Canonical Allele Identifier: CA384929084
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913612T>A (hg19) chr12:g.52519828T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519828T>A , CM000674.2:g.52519828T>A GRCh38
NC_000012.11:g.52913612T>A , CM000674.1:g.52913612T>A GRCh37
NC_000012.10:g.51199879T>A NCBI36
NG_008297.1:g.5632A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.469A>T MANE Select ENSP00000252242.4:p.Ile157Phe
ENST00000252242.8:c.469A>T ENSP00000252242.4:p.Ile157Phe
ENST00000549420.1:c.139A>T ENSP00000447209.1:p.Ile47Phe
ENST00000551275.1:c.364A>T ENSP00000448041.1:p.Ile122Phe
ENST00000552629.5:n.567A>T
NM_000424.3:c.469A>T NP_000415.2:p.Ile157Phe
NM_000424.4:c.469A>T MANE Select NP_000415.2:p.Ile157Phe
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