Canonical Allele Identifier: CA480069659
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1592193656
gnomAD v4: 12-52516696-C-T
MyVariant Identifiers: chr12:g.52910480C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516696C>T , CM000674.2:g.52516696C>T GRCh38
NC_000012.11:g.52910480C>T , CM000674.1:g.52910480C>T GRCh37
NC_000012.10:g.51196747C>T NCBI36
NG_008297.1:g.8764G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1380G>A MANE Select ENSP00000252242.4:p.Lys460=
ENST00000252242.8:c.1380G>A ENSP00000252242.4:p.Lys460=
ENST00000547890.5:n.758G>A
ENST00000548409.5:c.502G>A
ENST00000549511.5:n.587G>A
ENST00000552629.5:n.1478G>A
NM_000424.3:c.1380G>A NP_000415.2:p.Lys460=
NM_000424.4:c.1380G>A MANE Select NP_000415.2:p.Lys460=
Search 100 bp 5'
Search 100 bp 3'