Canonical Allele Identifier: CA2036540422
Gene: KRT5 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.550G= MANE Select ENSP00000252242.4:p.Asp184=
ENST00000252242.8:c.550G= ENSP00000252242.4:p.Asp184=
ENST00000549420.1:c.220G= ENSP00000447209.1:p.Asp74=
ENST00000552629.5:n.648G=
NM_000424.3:c.550G= NP_000415.2:p.Asp184=
NM_000424.4:c.550G= MANE Select NP_000415.2:p.Asp184=