Canonical Allele Identifier: CA384929167
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52519853-A-C
MyVariant Identifiers: chr12:g.52913637A>C (hg19) chr12:g.52519853A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519853A>C , CM000674.2:g.52519853A>C GRCh38
NC_000012.11:g.52913637A>C , CM000674.1:g.52913637A>C GRCh37
NC_000012.10:g.51199904A>C NCBI36
NG_008297.1:g.5607T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.444T>G MANE Select ENSP00000252242.4:p.Ser148Arg
ENST00000252242.8:c.444T>G ENSP00000252242.4:p.Ser148Arg
ENST00000549420.1:c.114T>G ENSP00000447209.1:p.Ser38Arg
ENST00000551275.1:c.339T>G ENSP00000448041.1:p.Ser113Arg
ENST00000552629.5:n.542T>G
NM_000424.3:c.444T>G NP_000415.2:p.Ser148Arg
NM_000424.4:c.444T>G MANE Select NP_000415.2:p.Ser148Arg
Search 100 bp 5'
Search 100 bp 3'