Canonical Allele Identifier: CA480070295
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913529G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519745G>A , CM000674.2:g.52519745G>A GRCh38
NC_000012.11:g.52913529G>A , CM000674.1:g.52913529G>A GRCh37
NC_000012.10:g.51199796G>A NCBI36
NG_008297.1:g.5715C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.552C>T MANE Select ENSP00000252242.4:p.Asp184=
ENST00000252242.8:c.552C>T ENSP00000252242.4:p.Asp184=
ENST00000549420.1:c.222C>T ENSP00000447209.1:p.Asp74=
ENST00000552629.5:n.650C>T
NM_000424.3:c.552C>T NP_000415.2:p.Asp184=
NM_000424.4:c.552C>T MANE Select NP_000415.2:p.Asp184=
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