Canonical Allele Identifier: CA2036540772
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520409A= , CM000674.2:g.52520409A= GRCh38
NC_000012.11:g.52914193A= , CM000674.1:g.52914193A= GRCh37
NC_000012.10:g.51200460A= NCBI36
NG_008297.1:g.5051T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.8:c.-113T= ENSP00000252242.4:n.-113T=
ENST00000546577.1:c.-25T= ENSP00000449651.1:n.-25T=
NM_000424.3:c.-113T= NP_000415.2:n.-113T=