Canonical Allele Identifier: CA384929184
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519854C>T , CM000674.2:g.52519854C>T GRCh38
NC_000012.11:g.52913638C>T , CM000674.1:g.52913638C>T GRCh37
NC_000012.10:g.51199905C>T NCBI36
NG_008297.1:g.5606G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.443G>A MANE Select ENSP00000252242.4:p.Ser148Asn
ENST00000252242.8:c.443G>A ENSP00000252242.4:p.Ser148Asn
ENST00000549420.1:c.113G>A ENSP00000447209.1:p.Ser38Asn
ENST00000551275.1:c.338G>A ENSP00000448041.1:p.Ser113Asn
ENST00000552629.5:n.541G>A
NM_000424.3:c.443G>A NP_000415.2:p.Ser148Asn
NM_000424.4:c.443G>A MANE Select NP_000415.2:p.Ser148Asn