Canonical Allele Identifier: CA2036538921
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516653C= , CM000674.2:g.52516653C= GRCh38
NC_000012.11:g.52910437C= , CM000674.1:g.52910437C= GRCh37
NC_000012.10:g.51196704C= NCBI36
NG_008297.1:g.8807G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.1423G= MANE Select ENSP00000252242.4:p.Glu475=
ENST00000252242.8:c.1423G= ENSP00000252242.4:p.Glu475=
ENST00000548409.5:c.545G=
ENST00000549511.5:n.630G=
ENST00000552629.5:n.1521G=
NM_000424.3:c.1423G= NP_000415.2:p.Glu475=
NM_000424.4:c.1423G= MANE Select NP_000415.2:p.Glu475=