Canonical Allele Identifier: CA2618932954
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520333_52520334del , CM000674.2:g.52520333_52520334del GRCh38
NC_000012.11:g.52914117_52914118del , CM000674.1:g.52914117_52914118del GRCh37
NC_000012.10:g.51200384_51200385del NCBI36
NG_008297.1:g.5126_5127del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.-38_-37del MANE Select ENSP00000252242.4:n.-38_-37del
ENST00000252242.8:c.-38_-37del ENSP00000252242.4:n.-38_-37del
ENST00000546577.1:c.-12-26_-12-25del ENSP00000449651.1:n.-12-26_-12-25del
ENST00000549420.1:c.-38_-37del ENSP00000447209.1:n.-38_-37del
ENST00000551275.1:c.-38_-37del ENSP00000448041.1:n.-38_-37del
ENST00000552629.5:n.61_62del
NM_000424.3:c.-38_-37del NP_000415.2:n.-38_-37del
NM_000424.4:c.-38_-37del MANE Select NP_000415.2:n.-38_-37del