Canonical Allele Identifier: CA216738
Gene: KRT5 HGNC NCBI

Linked Data

ClinVar Variation Id: 14643
dbSNP Id: rs58163069

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519778C>G , CM000674.2:g.52519778C>G GRCh38
NC_000012.11:g.52913562C>G , CM000674.1:g.52913562C>G GRCh37
NC_000012.10:g.51199829C>G NCBI36
NG_008297.1:g.5682G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.519G>C MANE Select ENSP00000252242.4:p.Lys173Asn
ENST00000252242.8:c.519G>C ENSP00000252242.4:p.Lys173Asn
ENST00000549420.1:c.189G>C ENSP00000447209.1:p.Lys63Asn
ENST00000551275.1:c.414G>C ENSP00000448041.1:p.Lys138Asn
ENST00000552629.5:n.617G>C
NM_000424.3:c.519G>C NP_000415.2:p.Lys173Asn
NM_000424.4:c.519G>C MANE Select NP_000415.2:p.Lys173Asn