Canonical Allele Identifier: CA384931027
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520202A>C , CM000674.2:g.52520202A>C GRCh38
NC_000012.11:g.52913986A>C , CM000674.1:g.52913986A>C GRCh37
NC_000012.10:g.51200253A>C NCBI36
NG_008297.1:g.5258T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.95T>G MANE Select ENSP00000252242.4:p.Phe32Cys
ENST00000252242.8:c.95T>G ENSP00000252242.4:p.Phe32Cys
ENST00000546577.1:c.95T>G ENSP00000449651.1:p.Phe32Cys
ENST00000549420.1:c.43+52T>G ENSP00000447209.1:n.43+52T>G
ENST00000551275.1:c.95T>G ENSP00000448041.1:p.Phe32Cys
ENST00000552629.5:n.193T>G
NM_000424.3:c.95T>G NP_000415.2:p.Phe32Cys
NM_000424.4:c.95T>G MANE Select NP_000415.2:p.Phe32Cys