Canonical Allele Identifier: CA689831271

Gene: KRT5

Linked Data

• dbSNP Id: rs1206727326
• MyVariant Identifiers: chr12:g.52910210_52910211del (hg19) ; chr12:g.52516426_52516427del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516426_52516427del , CM000674.2:g.52516426_52516427del	GRCh38
NC_000012.11:g.52910210_52910211del , CM000674.1:g.52910210_52910211del	GRCh37
NC_000012.10:g.51196477_51196478del	NCBI36
NG_008297.1:g.9033_9034del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1439+210_1439+211del MANE Select	ENSP00000252242.4:n.1439+210_1439+211del
ENST00000252242.8:c.1439+210_1439+211del	ENSP00000252242.4:n.1439+210_1439+211del
ENST00000548409.5:c.561+210_561+211del
ENST00000549511.5:n.646+210_646+211del
ENST00000552629.5:n.1747_1748del
NM_000424.3:c.1439+210_1439+211del	NP_000415.2:n.1439+210_1439+211del
NM_000424.4:c.1439+210_1439+211del MANE Select	NP_000415.2:n.1439+210_1439+211del