Canonical Allele Identifier: CA384929076
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913610G>C (hg19) chr12:g.52519826G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519826G>C , CM000674.2:g.52519826G>C GRCh38
NC_000012.11:g.52913610G>C , CM000674.1:g.52913610G>C GRCh37
NC_000012.10:g.51199877G>C NCBI36
NG_008297.1:g.5634C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.471C>G MANE Select ENSP00000252242.4:p.Ile157Met
ENST00000252242.8:c.471C>G ENSP00000252242.4:p.Ile157Met
ENST00000549420.1:c.141C>G ENSP00000447209.1:p.Ile47Met
ENST00000551275.1:c.366C>G ENSP00000448041.1:p.Ile122Met
ENST00000552629.5:n.569C>G
NM_000424.3:c.471C>G NP_000415.2:p.Ile157Met
NM_000424.4:c.471C>G MANE Select NP_000415.2:p.Ile157Met
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