Canonical Allele Identifier: CA2618930990

Gene: KRT5

Linked Data

• gnomAD v4: 12-52516323-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516326del , CM000674.2:g.52516326del	GRCh38
NC_000012.11:g.52910110del , CM000674.1:g.52910110del	GRCh37
NC_000012.10:g.51196377del	NCBI36
NG_008297.1:g.9136del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1439+313del MANE Select	ENSP00000252242.4:n.1439+313del
ENST00000252242.8:c.1439+313del	ENSP00000252242.4:n.1439+313del
ENST00000548409.5:c.561+313del
ENST00000549511.5:n.646+313del
ENST00000552629.5:n.1850del
NM_000424.3:c.1439+313del	NP_000415.2:n.1439+313del
NM_000424.4:c.1439+313del MANE Select	NP_000415.2:n.1439+313del