Canonical Allele Identifier: CA2575165515
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520313_52520315del , CM000674.2:g.52520313_52520315del GRCh38
NC_000012.11:g.52914097_52914099del , CM000674.1:g.52914097_52914099del GRCh37
NC_000012.10:g.51200364_51200366del NCBI36
NG_008297.1:g.5148_5150del

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.-16_-14del MANE Select ENSP00000252242.4:n.-16_-14del
ENST00000252242.8:c.-16_-14del ENSP00000252242.4:n.-16_-14del
ENST00000546577.1:c.-12-4_-12-2del ENSP00000449651.1:n.-12-4_-12-2del
ENST00000549420.1:c.-16_-14del ENSP00000447209.1:n.-16_-14del
ENST00000551275.1:c.-16_-14del ENSP00000448041.1:n.-16_-14del
ENST00000552629.5:n.83_85del
NM_000424.3:c.-16_-14del NP_000415.2:n.-16_-14del
NM_000424.4:c.-16_-14del MANE Select NP_000415.2:n.-16_-14del