Canonical Allele Identifier: CA384923464
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52910442A>G (hg19) chr12:g.52516658A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516658A>G , CM000674.2:g.52516658A>G GRCh38
NC_000012.11:g.52910442A>G , CM000674.1:g.52910442A>G GRCh37
NC_000012.10:g.51196709A>G NCBI36
NG_008297.1:g.8802T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1418T>C MANE Select ENSP00000252242.4:p.Leu473Pro
ENST00000252242.8:c.1418T>C ENSP00000252242.4:p.Leu473Pro
ENST00000548409.5:c.540T>C
ENST00000549511.5:n.625T>C
ENST00000552629.5:n.1516T>C
NM_000424.3:c.1418T>C NP_000415.2:p.Leu473Pro
NM_000424.4:c.1418T>C MANE Select NP_000415.2:p.Leu473Pro
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