Canonical Allele Identifier: CA384929430
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913683G>C (hg19) chr12:g.52519899G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519899G>C , CM000674.2:g.52519899G>C GRCh38
NC_000012.11:g.52913683G>C , CM000674.1:g.52913683G>C GRCh37
NC_000012.10:g.51199950G>C NCBI36
NG_008297.1:g.5561C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.398C>G MANE Select ENSP00000252242.4:p.Pro133Arg
ENST00000252242.8:c.398C>G ENSP00000252242.4:p.Pro133Arg
ENST00000549420.1:c.68C>G ENSP00000447209.1:p.Pro23Arg
ENST00000551275.1:c.293C>G ENSP00000448041.1:p.Pro98Arg
ENST00000552629.5:n.496C>G
NM_000424.3:c.398C>G NP_000415.2:p.Pro133Arg
NM_000424.4:c.398C>G MANE Select NP_000415.2:p.Pro133Arg
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Search 100 bp 3'