Canonical Allele Identifier: CA2036538773
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1938609980
gnomAD v4: 12-52516398-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516399del , CM000674.2:g.52516399del GRCh38
NC_000012.11:g.52910183del , CM000674.1:g.52910183del GRCh37
NC_000012.10:g.51196450del NCBI36
NG_008297.1:g.9061del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1439+238del MANE Select ENSP00000252242.4:n.1439+238del
ENST00000252242.8:c.1439+238del ENSP00000252242.4:n.1439+238del
ENST00000548409.5:c.561+238del
ENST00000549511.5:n.646+238del
ENST00000552629.5:n.1775del
NM_000424.3:c.1439+238del NP_000415.2:n.1439+238del
NM_000424.4:c.1439+238del MANE Select NP_000415.2:n.1439+238del
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