Canonical Allele Identifier: CA384929268
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519866G>T , CM000674.2:g.52519866G>T GRCh38
NC_000012.11:g.52913650G>T , CM000674.1:g.52913650G>T GRCh37
NC_000012.10:g.51199917G>T NCBI36
NG_008297.1:g.5594C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.431C>A MANE Select ENSP00000252242.4:p.Thr144Asn
ENST00000252242.8:c.431C>A ENSP00000252242.4:p.Thr144Asn
ENST00000549420.1:c.101C>A ENSP00000447209.1:p.Thr34Asn
ENST00000551275.1:c.326C>A ENSP00000448041.1:p.Thr109Asn
ENST00000552629.5:n.529C>A
NM_000424.3:c.431C>A NP_000415.2:p.Thr144Asn
NM_000424.4:c.431C>A MANE Select NP_000415.2:p.Thr144Asn