Canonical Allele Identifier: CA6582826
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs751505210

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519747C>T , CM000674.2:g.52519747C>T GRCh38
NC_000012.11:g.52913531C>T , CM000674.1:g.52913531C>T GRCh37
NC_000012.10:g.51199798C>T NCBI36
NG_008297.1:g.5713G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.550G>A MANE Select ENSP00000252242.4:p.Asp184Asn
ENST00000252242.8:c.550G>A ENSP00000252242.4:p.Asp184Asn
ENST00000549420.1:c.220G>A ENSP00000447209.1:p.Asp74Asn
ENST00000552629.5:n.648G>A
NM_000424.3:c.550G>A NP_000415.2:p.Asp184Asn
NM_000424.4:c.550G>A MANE Select NP_000415.2:p.Asp184Asn