Canonical Allele Identifier: CA2618932582
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519655C>A , CM000674.2:g.52519655C>A GRCh38
NC_000012.11:g.52913439C>A , CM000674.1:g.52913439C>A GRCh37
NC_000012.10:g.51199706C>A NCBI36
NG_008297.1:g.5805G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.555+87G>T MANE Select ENSP00000252242.4:n.555+87G>T
ENST00000252242.8:c.555+87G>T ENSP00000252242.4:n.555+87G>T
ENST00000549420.1:c.225+87G>T ENSP00000447209.1:n.225+87G>T
ENST00000552629.5:n.653+87G>T
NM_000424.3:c.555+87G>T NP_000415.2:n.555+87G>T
NM_000424.4:c.555+87G>T MANE Select NP_000415.2:n.555+87G>T