Canonical Allele Identifier: CA384923865
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52910512G>T (hg19) chr12:g.52516728G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516728G>T , CM000674.2:g.52516728G>T GRCh38
NC_000012.11:g.52910512G>T , CM000674.1:g.52910512G>T GRCh37
NC_000012.10:g.51196779G>T NCBI36
NG_008297.1:g.8732C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1348C>A MANE Select ENSP00000252242.4:p.Leu450Met
ENST00000252242.8:c.1348C>A ENSP00000252242.4:p.Leu450Met
ENST00000547890.5:n.726C>A
ENST00000548409.5:c.470C>A
ENST00000549511.5:n.555C>A
ENST00000552629.5:n.1446C>A
NM_000424.3:c.1348C>A NP_000415.2:p.Leu450Met
NM_000424.4:c.1348C>A MANE Select NP_000415.2:p.Leu450Met
Search 100 bp 5'
Search 100 bp 3'