Canonical Allele Identifier: CA6582561
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs371739329

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516786G>C , CM000674.2:g.52516786G>C GRCh38
NC_000012.11:g.52910570G>C , CM000674.1:g.52910570G>C GRCh37
NC_000012.10:g.51196837G>C NCBI36
NG_008297.1:g.8674C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1290C>G MANE Select ENSP00000252242.4:p.Asn430Lys
ENST00000252242.8:c.1290C>G ENSP00000252242.4:p.Asn430Lys
ENST00000547890.5:n.668C>G
ENST00000548409.5:c.412C>G
ENST00000549511.5:n.497C>G
ENST00000552629.5:n.1388C>G
NM_000424.3:c.1290C>G NP_000415.2:p.Asn430Lys
NM_000424.4:c.1290C>G MANE Select NP_000415.2:p.Asn430Lys