Canonical Allele Identifier: CA2036540492
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519872T= , CM000674.2:g.52519872T= GRCh38
NC_000012.11:g.52913656T= , CM000674.1:g.52913656T= GRCh37
NC_000012.10:g.51199923T= NCBI36
NG_008297.1:g.5588A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.425A= MANE Select ENSP00000252242.4:p.Glu142=
ENST00000252242.8:c.425A= ENSP00000252242.4:p.Glu142=
ENST00000549420.1:c.95A= ENSP00000447209.1:p.Glu32=
ENST00000551275.1:c.320A= ENSP00000448041.1:p.Glu107=
ENST00000552629.5:n.523A=
NM_000424.3:c.425A= NP_000415.2:p.Glu142=
NM_000424.4:c.425A= MANE Select NP_000415.2:p.Glu142=