Canonical Allele Identifier: CA384928743
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913535G>T (hg19) chr12:g.52519751G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519751G>T , CM000674.2:g.52519751G>T GRCh38
NC_000012.11:g.52913535G>T , CM000674.1:g.52913535G>T GRCh37
NC_000012.10:g.51199802G>T NCBI36
NG_008297.1:g.5709C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.546C>A MANE Select ENSP00000252242.4:p.Phe182Leu
ENST00000252242.8:c.546C>A ENSP00000252242.4:p.Phe182Leu
ENST00000549420.1:c.216C>A ENSP00000447209.1:p.Phe72Leu
ENST00000551275.1:c.441C>A ENSP00000448041.1:p.Phe147Leu
ENST00000552629.5:n.644C>A
NM_000424.3:c.546C>A NP_000415.2:p.Phe182Leu
NM_000424.4:c.546C>A MANE Select NP_000415.2:p.Phe182Leu
Search 100 bp 5'
Search 100 bp 3'