Canonical Allele Identifier: CA480070366
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913655C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519871C>T , CM000674.2:g.52519871C>T GRCh38
NC_000012.11:g.52913655C>T , CM000674.1:g.52913655C>T GRCh37
NC_000012.10:g.51199922C>T NCBI36
NG_008297.1:g.5589G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.426G>A MANE Select ENSP00000252242.4:p.Glu142=
ENST00000252242.8:c.426G>A ENSP00000252242.4:p.Glu142=
ENST00000549420.1:c.96G>A ENSP00000447209.1:p.Glu32=
ENST00000551275.1:c.321G>A ENSP00000448041.1:p.Glu107=
ENST00000552629.5:n.524G>A
NM_000424.3:c.426G>A NP_000415.2:p.Glu142=
NM_000424.4:c.426G>A MANE Select NP_000415.2:p.Glu142=
Search 100 bp 5'
Search 100 bp 3'