Canonical Allele Identifier: CA384928720
Gene: KRT5 HGNC NCBI

Linked Data

COSMIC: COSM325649
MyVariant Identifiers: chr12:g.52913530T>A (hg19) chr12:g.52519746T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519746T>A , CM000674.2:g.52519746T>A GRCh38
NC_000012.11:g.52913530T>A , CM000674.1:g.52913530T>A GRCh37
NC_000012.10:g.51199797T>A NCBI36
NG_008297.1:g.5714A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.551A>T MANE Select ENSP00000252242.4:p.Asp184Val
ENST00000252242.8:c.551A>T ENSP00000252242.4:p.Asp184Val
ENST00000549420.1:c.221A>T ENSP00000447209.1:p.Asp74Val
ENST00000552629.5:n.649A>T
NM_000424.3:c.551A>T NP_000415.2:p.Asp184Val
NM_000424.4:c.551A>T MANE Select NP_000415.2:p.Asp184Val
Search 100 bp 5'
Search 100 bp 3'