Canonical Allele Identifier: CA384927923
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52912919T>A (hg19) chr12:g.52519135T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519135T>A , CM000674.2:g.52519135T>A GRCh38
NC_000012.11:g.52912919T>A , CM000674.1:g.52912919T>A GRCh37
NC_000012.10:g.51199186T>A NCBI36
NG_008297.1:g.6325A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.581A>T MANE Select ENSP00000252242.4:p.Lys194Met
ENST00000252242.8:c.581A>T ENSP00000252242.4:p.Lys194Met
ENST00000549420.1:c.251A>T ENSP00000447209.1:p.Lys84Met
ENST00000551013.1:n.109A>T
ENST00000552629.5:n.679A>T
NM_000424.3:c.581A>T NP_000415.2:p.Lys194Met
NM_000424.4:c.581A>T MANE Select NP_000415.2:p.Lys194Met
Search 100 bp 5'
Search 100 bp 3'