Canonical Allele Identifier: CA2036539045
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516884_52516889delinsGTTGCT , CM000674.2:g.52516884_52516889delinsGTTGCT GRCh38
NC_000012.11:g.52910668_52910673delinsGTTGCT , CM000674.1:g.52910668_52910673delinsGTTGCT GRCh37
NC_000012.10:g.51196935_51196940delinsGTTGCT NCBI36
NG_008297.1:g.8571_8576delinsAGCAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1219-32_1219-27delinsAGCAAC MANE Select ENSP00000252242.4:n.1219-32_1219-27delinsAGCAAC
ENST00000252242.8:c.1219-32_1219-27delinsAGCAAC ENSP00000252242.4:n.1219-32_1219-27delinsAGCAAC
ENST00000547890.5:n.565_570delinsAGCAAC
ENST00000548409.5:c.341-32_341-27delinsAGCAAC
ENST00000549511.5:n.426-32_426-27delinsAGCAAC
ENST00000552629.5:n.1317-32_1317-27delinsAGCAAC
NM_000424.3:c.1219-32_1219-27delinsAGCAAC NP_000415.2:n.1219-32_1219-27delinsAGCAAC
NM_000424.4:c.1219-32_1219-27delinsAGCAAC MANE Select NP_000415.2:n.1219-32_1219-27delinsAGCAAC