Canonical Allele Identifier: CA2036538936
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516682A= , CM000674.2:g.52516682A= GRCh38
NC_000012.11:g.52910466A= , CM000674.1:g.52910466A= GRCh37
NC_000012.10:g.51196733A= NCBI36
NG_008297.1:g.8778T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1394T= MANE Select ENSP00000252242.4:p.Val465=
ENST00000252242.8:c.1394T= ENSP00000252242.4:p.Val465=
ENST00000548409.5:c.516T=
ENST00000549511.5:n.601T=
ENST00000552629.5:n.1492T=
NM_000424.3:c.1394T= NP_000415.2:p.Val465=
NM_000424.4:c.1394T= MANE Select NP_000415.2:p.Val465=