Canonical Allele Identifier: CA2838935824
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516584G>T , CM000674.2:g.52516584G>T GRCh38
NC_000012.11:g.52910368G>T , CM000674.1:g.52910368G>T GRCh37
NC_000012.10:g.51196635G>T NCBI36
NG_008297.1:g.8876C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1439+53C>A MANE Select ENSP00000252242.4:n.1439+53C>A
ENST00000252242.8:c.1439+53C>A ENSP00000252242.4:n.1439+53C>A
ENST00000548409.5:c.561+53C>A
ENST00000549511.5:n.646+53C>A
ENST00000552629.5:n.1590C>A
NM_000424.3:c.1439+53C>A NP_000415.2:n.1439+53C>A
NM_000424.4:c.1439+53C>A MANE Select NP_000415.2:n.1439+53C>A