Canonical Allele Identifier: CA2036538920
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516652T= , CM000674.2:g.52516652T= GRCh38
NC_000012.11:g.52910436T= , CM000674.1:g.52910436T= GRCh37
NC_000012.10:g.51196703T= NCBI36
NG_008297.1:g.8808A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.1424A= MANE Select ENSP00000252242.4:p.Glu475=
ENST00000252242.8:c.1424A= ENSP00000252242.4:p.Glu475=
ENST00000548409.5:c.546A=
ENST00000549511.5:n.631A=
ENST00000552629.5:n.1522A=
NM_000424.3:c.1424A= NP_000415.2:p.Glu475=
NM_000424.4:c.1424A= MANE Select NP_000415.2:p.Glu475=