Canonical Allele Identifier: CA384928697
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913525C>G (hg19) chr12:g.52519741C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519741C>G , CM000674.2:g.52519741C>G GRCh38
NC_000012.11:g.52913525C>G , CM000674.1:g.52913525C>G GRCh37
NC_000012.10:g.51199792C>G NCBI36
NG_008297.1:g.5719G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.555+1G>C MANE Select ENSP00000252242.4:n.555+1G>C
ENST00000252242.8:c.555+1G>C ENSP00000252242.4:n.555+1G>C
ENST00000549420.1:c.225+1G>C ENSP00000447209.1:n.225+1G>C
ENST00000552629.5:n.653+1G>C
NM_000424.3:c.555+1G>C NP_000415.2:n.555+1G>C
NM_000424.4:c.555+1G>C MANE Select NP_000415.2:n.555+1G>C
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