Canonical Allele Identifier: CA384929191
Gene: KRT5 HGNC NCBI

Linked Data

COSMIC: COSM4914777
MyVariant Identifiers: chr12:g.52913639T>A (hg19) chr12:g.52519855T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519855T>A , CM000674.2:g.52519855T>A GRCh38
NC_000012.11:g.52913639T>A , CM000674.1:g.52913639T>A GRCh37
NC_000012.10:g.51199906T>A NCBI36
NG_008297.1:g.5605A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.442A>T MANE Select ENSP00000252242.4:p.Ser148Cys
ENST00000252242.8:c.442A>T ENSP00000252242.4:p.Ser148Cys
ENST00000549420.1:c.112A>T ENSP00000447209.1:p.Ser38Cys
ENST00000551275.1:c.337A>T ENSP00000448041.1:p.Ser113Cys
ENST00000552629.5:n.540A>T
NM_000424.3:c.442A>T NP_000415.2:p.Ser148Cys
NM_000424.4:c.442A>T MANE Select NP_000415.2:p.Ser148Cys
Search 100 bp 5'
Search 100 bp 3'