Canonical Allele Identifier: CA384929311
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913660G>C (hg19) chr12:g.52519876G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519876G>C , CM000674.2:g.52519876G>C GRCh38
NC_000012.11:g.52913660G>C , CM000674.1:g.52913660G>C GRCh37
NC_000012.10:g.51199927G>C NCBI36
NG_008297.1:g.5584C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.421C>G MANE Select ENSP00000252242.4:p.Gln141Glu
ENST00000252242.8:c.421C>G ENSP00000252242.4:p.Gln141Glu
ENST00000549420.1:c.91C>G ENSP00000447209.1:p.Gln31Glu
ENST00000551275.1:c.316C>G ENSP00000448041.1:p.Gln106Glu
ENST00000552629.5:n.519C>G
NM_000424.3:c.421C>G NP_000415.2:p.Gln141Glu
NM_000424.4:c.421C>G MANE Select NP_000415.2:p.Gln141Glu
Search 100 bp 5'
Search 100 bp 3'