Canonical Allele Identifier: CA2832565176

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516452dup , CM000674.2:g.52516452dup	GRCh38
NC_000012.11:g.52910236dup , CM000674.1:g.52910236dup	GRCh37
NC_000012.10:g.51196503dup	NCBI36
NG_008297.1:g.9012dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1439+189dup MANE Select	ENSP00000252242.4:n.1439+189dup
ENST00000252242.8:c.1439+189dup	ENSP00000252242.4:n.1439+189dup
ENST00000548409.5:c.561+189dup
ENST00000549511.5:n.646+189dup
ENST00000552629.5:n.1726dup
NM_000424.3:c.1439+189dup	NP_000415.2:n.1439+189dup
NM_000424.4:c.1439+189dup MANE Select	NP_000415.2:n.1439+189dup