Canonical Allele Identifier: CA2618932594
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519671C>T , CM000674.2:g.52519671C>T GRCh38
NC_000012.11:g.52913455C>T , CM000674.1:g.52913455C>T GRCh37
NC_000012.10:g.51199722C>T NCBI36
NG_008297.1:g.5789G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.555+71G>A MANE Select ENSP00000252242.4:n.555+71G>A
ENST00000252242.8:c.555+71G>A ENSP00000252242.4:n.555+71G>A
ENST00000549420.1:c.225+71G>A ENSP00000447209.1:n.225+71G>A
ENST00000552629.5:n.653+71G>A
NM_000424.3:c.555+71G>A NP_000415.2:n.555+71G>A
NM_000424.4:c.555+71G>A MANE Select NP_000415.2:n.555+71G>A