Canonical Allele Identifier: CA384929883
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913768A>T (hg19) chr12:g.52519984A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519984A>T , CM000674.2:g.52519984A>T GRCh38
NC_000012.11:g.52913768A>T , CM000674.1:g.52913768A>T GRCh37
NC_000012.10:g.51200035A>T NCBI36
NG_008297.1:g.5476T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.313T>A MANE Select ENSP00000252242.4:p.Phe105Ile
ENST00000252242.8:c.313T>A ENSP00000252242.4:p.Phe105Ile
ENST00000546577.1:c.313T>A ENSP00000449651.1:p.Phe105Ile
ENST00000549420.1:c.44-61T>A ENSP00000447209.1:n.44-61T>A
ENST00000551275.1:c.208T>A ENSP00000448041.1:p.Phe70Ile
ENST00000552629.5:n.411T>A
NM_000424.3:c.313T>A NP_000415.2:p.Phe105Ile
NM_000424.4:c.313T>A MANE Select NP_000415.2:p.Phe105Ile
Search 100 bp 5'
Search 100 bp 3'