Canonical Allele Identifier: CA384928711
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519744T>A , CM000674.2:g.52519744T>A GRCh38
NC_000012.11:g.52913528T>A , CM000674.1:g.52913528T>A GRCh37
NC_000012.10:g.51199795T>A NCBI36
NG_008297.1:g.5716A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.553A>T MANE Select ENSP00000252242.4:p.Lys185Ter
ENST00000252242.8:c.553A>T ENSP00000252242.4:p.Lys185Ter
ENST00000549420.1:c.223A>T ENSP00000447209.1:p.Lys75Ter
ENST00000552629.5:n.651A>T
NM_000424.3:c.553A>T NP_000415.2:p.Lys185Ter
NM_000424.4:c.553A>T MANE Select NP_000415.2:p.Lys185Ter