Canonical Allele Identifier: CA384928751
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913537A>T (hg19) chr12:g.52519753A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519753A>T , CM000674.2:g.52519753A>T GRCh38
NC_000012.11:g.52913537A>T , CM000674.1:g.52913537A>T GRCh37
NC_000012.10:g.51199804A>T NCBI36
NG_008297.1:g.5707T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.544T>A MANE Select ENSP00000252242.4:p.Phe182Ile
ENST00000252242.8:c.544T>A ENSP00000252242.4:p.Phe182Ile
ENST00000549420.1:c.214T>A ENSP00000447209.1:p.Phe72Ile
ENST00000551275.1:c.439T>A ENSP00000448041.1:p.Phe147Ile
ENST00000552629.5:n.642T>A
NM_000424.3:c.544T>A NP_000415.2:p.Phe182Ile
NM_000424.4:c.544T>A MANE Select NP_000415.2:p.Phe182Ile
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