Canonical Allele Identifier: CA2036538941
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516695G= , CM000674.2:g.52516695G= GRCh38
NC_000012.11:g.52910479G= , CM000674.1:g.52910479G= GRCh37
NC_000012.10:g.51196746G= NCBI36
NG_008297.1:g.8765C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1381C= MANE Select ENSP00000252242.4:p.Leu461=
ENST00000252242.8:c.1381C= ENSP00000252242.4:p.Leu461=
ENST00000547890.5:n.759C=
ENST00000548409.5:c.503C=
ENST00000549511.5:n.588C=
ENST00000552629.5:n.1479C=
NM_000424.3:c.1381C= NP_000415.2:p.Leu461=
NM_000424.4:c.1381C= MANE Select NP_000415.2:p.Leu461=