Canonical Allele Identifier: CA384929232
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913642G>C (hg19) chr12:g.52519858G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519858G>C , CM000674.2:g.52519858G>C GRCh38
NC_000012.11:g.52913642G>C , CM000674.1:g.52913642G>C GRCh37
NC_000012.10:g.51199909G>C NCBI36
NG_008297.1:g.5602C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.439C>G MANE Select ENSP00000252242.4:p.Gln147Glu
ENST00000252242.8:c.439C>G ENSP00000252242.4:p.Gln147Glu
ENST00000549420.1:c.109C>G ENSP00000447209.1:p.Gln37Glu
ENST00000551275.1:c.334C>G ENSP00000448041.1:p.Gln112Glu
ENST00000552629.5:n.537C>G
NM_000424.3:c.439C>G NP_000415.2:p.Gln147Glu
NM_000424.4:c.439C>G MANE Select NP_000415.2:p.Gln147Glu
Search 100 bp 5'
Search 100 bp 3'