Canonical Allele Identifier: CA384927905
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519129A>C , CM000674.2:g.52519129A>C GRCh38
NC_000012.11:g.52912913A>C , CM000674.1:g.52912913A>C GRCh37
NC_000012.10:g.51199180A>C NCBI36
NG_008297.1:g.6331T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.587T>G MANE Select ENSP00000252242.4:p.Leu196Arg
ENST00000252242.8:c.587T>G ENSP00000252242.4:p.Leu196Arg
ENST00000549420.1:c.257T>G ENSP00000447209.1:p.Leu86Arg
ENST00000551013.1:n.115T>G
ENST00000552629.5:n.685T>G
NM_000424.3:c.587T>G NP_000415.2:p.Leu196Arg
NM_000424.4:c.587T>G MANE Select NP_000415.2:p.Leu196Arg