Canonical Allele Identifier: CA2036540385
Gene: KRT5 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519670T= , CM000674.2:g.52519670T= GRCh38
NC_000012.11:g.52913454T= , CM000674.1:g.52913454T= GRCh37
NC_000012.10:g.51199721T= NCBI36
NG_008297.1:g.5790A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.555+72A= MANE Select ENSP00000252242.4:n.555+72A=
ENST00000252242.8:c.555+72A= ENSP00000252242.4:n.555+72A=
ENST00000549420.1:c.225+72A= ENSP00000447209.1:n.225+72A=
ENST00000552629.5:n.653+72A=
NM_000424.3:c.555+72A= NP_000415.2:n.555+72A=
NM_000424.4:c.555+72A= MANE Select NP_000415.2:n.555+72A=
Search 100 bp 5'
Search 100 bp 3'