Canonical Allele Identifier: CA384928708
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913527T>G (hg19) chr12:g.52519743T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519743T>G , CM000674.2:g.52519743T>G GRCh38
NC_000012.11:g.52913527T>G , CM000674.1:g.52913527T>G GRCh37
NC_000012.10:g.51199794T>G NCBI36
NG_008297.1:g.5717A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.554A>C MANE Select ENSP00000252242.4:p.Lys185Thr
ENST00000252242.8:c.554A>C ENSP00000252242.4:p.Lys185Thr
ENST00000549420.1:c.224A>C ENSP00000447209.1:p.Lys75Thr
ENST00000552629.5:n.652A>C
NM_000424.3:c.554A>C NP_000415.2:p.Lys185Thr
NM_000424.4:c.554A>C MANE Select NP_000415.2:p.Lys185Thr
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