Canonical Allele Identifier: CA384929374
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913675G>A (hg19) chr12:g.52519891G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519891G>A , CM000674.2:g.52519891G>A GRCh38
NC_000012.11:g.52913675G>A , CM000674.1:g.52913675G>A GRCh37
NC_000012.10:g.51199942G>A NCBI36
NG_008297.1:g.5569C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.406C>T MANE Select ENSP00000252242.4:p.Pro136Ser
ENST00000252242.8:c.406C>T ENSP00000252242.4:p.Pro136Ser
ENST00000549420.1:c.76C>T ENSP00000447209.1:p.Pro26Ser
ENST00000551275.1:c.301C>T ENSP00000448041.1:p.Pro101Ser
ENST00000552629.5:n.504C>T
NM_000424.3:c.406C>T NP_000415.2:p.Pro136Ser
NM_000424.4:c.406C>T MANE Select NP_000415.2:p.Pro136Ser
Search 100 bp 5'
Search 100 bp 3'