Canonical Allele Identifier: CA384928722
Gene: KRT5 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.551A>G MANE Select ENSP00000252242.4:p.Asp184Gly
ENST00000252242.8:c.551A>G ENSP00000252242.4:p.Asp184Gly
ENST00000549420.1:c.221A>G ENSP00000447209.1:p.Asp74Gly
ENST00000552629.5:n.649A>G
NM_000424.3:c.551A>G NP_000415.2:p.Asp184Gly
NM_000424.4:c.551A>G MANE Select NP_000415.2:p.Asp184Gly
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Search 100 bp 3'