Canonical Allele Identifier: CA384929378
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52519891-G-T
MyVariant Identifiers: chr12:g.52913675G>T (hg19) chr12:g.52519891G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519891G>T , CM000674.2:g.52519891G>T GRCh38
NC_000012.11:g.52913675G>T , CM000674.1:g.52913675G>T GRCh37
NC_000012.10:g.51199942G>T NCBI36
NG_008297.1:g.5569C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.406C>A MANE Select ENSP00000252242.4:p.Pro136Thr
ENST00000252242.8:c.406C>A ENSP00000252242.4:p.Pro136Thr
ENST00000549420.1:c.76C>A ENSP00000447209.1:p.Pro26Thr
ENST00000551275.1:c.301C>A ENSP00000448041.1:p.Pro101Thr
ENST00000552629.5:n.504C>A
NM_000424.3:c.406C>A NP_000415.2:p.Pro136Thr
NM_000424.4:c.406C>A MANE Select NP_000415.2:p.Pro136Thr
Search 100 bp 5'
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