Canonical Allele Identifier: CA384929247
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913644T>G (hg19) chr12:g.52519860T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519860T>G , CM000674.2:g.52519860T>G GRCh38
NC_000012.11:g.52913644T>G , CM000674.1:g.52913644T>G GRCh37
NC_000012.10:g.51199911T>G NCBI36
NG_008297.1:g.5600A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.437A>C MANE Select ENSP00000252242.4:p.Asn146Thr
ENST00000252242.8:c.437A>C ENSP00000252242.4:p.Asn146Thr
ENST00000549420.1:c.107A>C ENSP00000447209.1:p.Asn36Thr
ENST00000551275.1:c.332A>C ENSP00000448041.1:p.Asn111Thr
ENST00000552629.5:n.535A>C
NM_000424.3:c.437A>C NP_000415.2:p.Asn146Thr
NM_000424.4:c.437A>C MANE Select NP_000415.2:p.Asn146Thr
Search 100 bp 5'
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