Canonical Allele Identifier: CA384923443
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52910436T>G (hg19) chr12:g.52516652T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516652T>G , CM000674.2:g.52516652T>G GRCh38
NC_000012.11:g.52910436T>G , CM000674.1:g.52910436T>G GRCh37
NC_000012.10:g.51196703T>G NCBI36
NG_008297.1:g.8808A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1424A>C MANE Select ENSP00000252242.4:p.Glu475Ala
ENST00000252242.8:c.1424A>C ENSP00000252242.4:p.Glu475Ala
ENST00000548409.5:c.546A>C
ENST00000549511.5:n.631A>C
ENST00000552629.5:n.1522A>C
NM_000424.3:c.1424A>C NP_000415.2:p.Glu475Ala
NM_000424.4:c.1424A>C MANE Select NP_000415.2:p.Glu475Ala
Search 100 bp 5'
Search 100 bp 3'