Canonical Allele Identifier: CA384930539
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520113T>A , CM000674.2:g.52520113T>A GRCh38
NC_000012.11:g.52913897T>A , CM000674.1:g.52913897T>A GRCh37
NC_000012.10:g.51200164T>A NCBI36
NG_008297.1:g.5347A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.184A>T MANE Select ENSP00000252242.4:p.Ser62Cys
ENST00000252242.8:c.184A>T ENSP00000252242.4:p.Ser62Cys
ENST00000546577.1:c.184A>T ENSP00000449651.1:p.Ser62Cys
ENST00000549420.1:c.43+141A>T ENSP00000447209.1:n.43+141A>T
ENST00000551275.1:c.172+12A>T ENSP00000448041.1:n.172+12A>T
ENST00000552629.5:n.282A>T
NM_000424.3:c.184A>T NP_000415.2:p.Ser62Cys
NM_000424.4:c.184A>T MANE Select NP_000415.2:p.Ser62Cys