Canonical Allele Identifier: CA2036538940
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516693C= , CM000674.2:g.52516693C= GRCh38
NC_000012.11:g.52910477C= , CM000674.1:g.52910477C= GRCh37
NC_000012.10:g.51196744C= NCBI36
NG_008297.1:g.8767G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1383G= MANE Select ENSP00000252242.4:p.Leu461=
ENST00000252242.8:c.1383G= ENSP00000252242.4:p.Leu461=
ENST00000547890.5:n.761G=
ENST00000548409.5:c.505G=
ENST00000549511.5:n.590G=
ENST00000552629.5:n.1481G=
NM_000424.3:c.1383G= NP_000415.2:p.Leu461=
NM_000424.4:c.1383G= MANE Select NP_000415.2:p.Leu461=