Canonical Allele Identifier: CA2036538746
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1938609277
gnomAD v4: 12-52516351-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516351C>T , CM000674.2:g.52516351C>T GRCh38
NC_000012.11:g.52910135C>T , CM000674.1:g.52910135C>T GRCh37
NC_000012.10:g.51196402C>T NCBI36
NG_008297.1:g.9109G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1439+286G>A MANE Select ENSP00000252242.4:n.1439+286G>A
ENST00000252242.8:c.1439+286G>A ENSP00000252242.4:n.1439+286G>A
ENST00000548409.5:c.561+286G>A
ENST00000549511.5:n.646+286G>A
ENST00000552629.5:n.1823G>A
NM_000424.3:c.1439+286G>A NP_000415.2:n.1439+286G>A
NM_000424.4:c.1439+286G>A MANE Select NP_000415.2:n.1439+286G>A
Search 100 bp 5'
Search 100 bp 3'