Canonical Allele Identifier: CA2618932985
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520368C>T , CM000674.2:g.52520368C>T GRCh38
NC_000012.11:g.52914152C>T , CM000674.1:g.52914152C>T GRCh37
NC_000012.10:g.51200419C>T NCBI36
NG_008297.1:g.5092G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.-72G>A MANE Select ENSP00000252242.4:n.-72G>A
ENST00000252242.8:c.-72G>A ENSP00000252242.4:n.-72G>A
ENST00000546577.1:c.-13+29G>A ENSP00000449651.1:n.-13+29G>A
ENST00000549420.1:c.-72G>A ENSP00000447209.1:n.-72G>A
ENST00000551275.1:c.-72G>A ENSP00000448041.1:n.-72G>A
ENST00000552629.5:n.27G>A
NM_000424.3:c.-72G>A NP_000415.2:n.-72G>A
NM_000424.4:c.-72G>A MANE Select NP_000415.2:n.-72G>A