Canonical Allele Identifier: CA384929714
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913735C>T (hg19) chr12:g.52519951C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519951C>T , CM000674.2:g.52519951C>T GRCh38
NC_000012.11:g.52913735C>T , CM000674.1:g.52913735C>T GRCh37
NC_000012.10:g.51200002C>T NCBI36
NG_008297.1:g.5509G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.346G>A MANE Select ENSP00000252242.4:p.Gly116Arg
ENST00000252242.8:c.346G>A ENSP00000252242.4:p.Gly116Arg
ENST00000546577.1:c.346G>A ENSP00000449651.1:p.Gly116Arg
ENST00000549420.1:c.44-28G>A ENSP00000447209.1:n.44-28G>A
ENST00000551275.1:c.241G>A ENSP00000448041.1:p.Gly81Arg
ENST00000552629.5:n.444G>A
NM_000424.3:c.346G>A NP_000415.2:p.Gly116Arg
NM_000424.4:c.346G>A MANE Select NP_000415.2:p.Gly116Arg
Search 100 bp 5'
Search 100 bp 3'