Canonical Allele Identifier: CA2036538945
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516701T= , CM000674.2:g.52516701T= GRCh38
NC_000012.11:g.52910485T= , CM000674.1:g.52910485T= GRCh37
NC_000012.10:g.51196752T= NCBI36
NG_008297.1:g.8759A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1375A= MANE Select ENSP00000252242.4:p.Thr459=
ENST00000252242.8:c.1375A= ENSP00000252242.4:p.Thr459=
ENST00000547890.5:n.753A=
ENST00000548409.5:c.497A=
ENST00000549511.5:n.582A=
ENST00000552629.5:n.1473A=
NM_000424.3:c.1375A= NP_000415.2:p.Thr459=
NM_000424.4:c.1375A= MANE Select NP_000415.2:p.Thr459=