Canonical Allele Identifier: CA2036538933
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516677T= , CM000674.2:g.52516677T= GRCh38
NC_000012.11:g.52910461T= , CM000674.1:g.52910461T= GRCh37
NC_000012.10:g.51196728T= NCBI36
NG_008297.1:g.8783A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1399A= MANE Select ENSP00000252242.4:p.Ile467=
ENST00000252242.8:c.1399A= ENSP00000252242.4:p.Ile467=
ENST00000548409.5:c.521A=
ENST00000549511.5:n.606A=
ENST00000552629.5:n.1497A=
NM_000424.3:c.1399A= NP_000415.2:p.Ile467=
NM_000424.4:c.1399A= MANE Select NP_000415.2:p.Ile467=