Canonical Allele Identifier: CA2618932924

Gene: KRT5

Linked Data

• gnomAD v4: 12-52520035-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520038del , CM000674.2:g.52520038del	GRCh38
NC_000012.11:g.52913822del , CM000674.1:g.52913822del	GRCh37
NC_000012.10:g.51200089del	NCBI36
NG_008297.1:g.5424del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.261del MANE Select	ENSP00000252242.4:p.Phe87LeufsTer?
ENST00000252242.8:c.261del	ENSP00000252242.4:p.Phe87LeufsTer?
ENST00000546577.1:c.261del	ENSP00000449651.1:p.Phe87LeufsTer?
ENST00000549420.1:c.44-113del	ENSP00000447209.1:n.44-113del
ENST00000551275.1:c.173-17del	ENSP00000448041.1:n.173-17del
ENST00000552629.5:n.359del
NM_000424.3:c.261del	NP_000415.2:p.Phe87LeufsTer?
NM_000424.4:c.261del MANE Select	NP_000415.2:p.Phe87LeufsTer?