Canonical Allele Identifier: CA384923610
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516685T>C , CM000674.2:g.52516685T>C GRCh38
NC_000012.11:g.52910469T>C , CM000674.1:g.52910469T>C GRCh37
NC_000012.10:g.51196736T>C NCBI36
NG_008297.1:g.8775A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1391A>G MANE Select ENSP00000252242.4:p.Asp464Gly
ENST00000252242.8:c.1391A>G ENSP00000252242.4:p.Asp464Gly
ENST00000548409.5:c.513A>G
ENST00000549511.5:n.598A>G
ENST00000552629.5:n.1489A>G
NM_000424.3:c.1391A>G NP_000415.2:p.Asp464Gly
NM_000424.4:c.1391A>G MANE Select NP_000415.2:p.Asp464Gly