Canonical Allele Identifier: CA2036538793

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516425_52516427delinsAGC , CM000674.2:g.52516425_52516427delinsAGC	GRCh38
NC_000012.11:g.52910209_52910211delinsAGC , CM000674.1:g.52910209_52910211delinsAGC	GRCh37
NC_000012.10:g.51196476_51196478delinsAGC	NCBI36
NG_008297.1:g.9033_9035delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1439+210_1439+212delinsGCT MANE Select	ENSP00000252242.4:n.1439+210_1439+212delinsGCT
ENST00000252242.8:c.1439+210_1439+212delinsGCT	ENSP00000252242.4:n.1439+210_1439+212delinsGCT
ENST00000548409.5:c.561+210_561+212delinsGCT
ENST00000549511.5:n.646+210_646+212delinsGCT
ENST00000552629.5:n.1747_1749delinsGCT
NM_000424.3:c.1439+210_1439+212delinsGCT	NP_000415.2:n.1439+210_1439+212delinsGCT
NM_000424.4:c.1439+210_1439+212delinsGCT MANE Select	NP_000415.2:n.1439+210_1439+212delinsGCT