Canonical Allele Identifier: CA2036540505
Gene: KRT5 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519897C= , CM000674.2:g.52519897C= GRCh38
NC_000012.11:g.52913681C= , CM000674.1:g.52913681C= GRCh37
NC_000012.10:g.51199948C= NCBI36
NG_008297.1:g.5563G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.400G= MANE Select ENSP00000252242.4:p.Val134=
ENST00000252242.8:c.400G= ENSP00000252242.4:p.Val134=
ENST00000549420.1:c.70G= ENSP00000447209.1:p.Val24=
ENST00000551275.1:c.295G= ENSP00000448041.1:p.Val99=
ENST00000552629.5:n.498G=
NM_000424.3:c.400G= NP_000415.2:p.Val134=
NM_000424.4:c.400G= MANE Select NP_000415.2:p.Val134=
Search 100 bp 5'
Search 100 bp 3'