Canonical Allele Identifier: CA2036538819

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516478G= , CM000674.2:g.52516478G=	GRCh38
NC_000012.11:g.52910262G= , CM000674.1:g.52910262G=	GRCh37
NC_000012.10:g.51196529G=	NCBI36
NG_008297.1:g.8982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1439+159C= MANE Select	ENSP00000252242.4:n.1439+159C=
ENST00000252242.8:c.1439+159C=	ENSP00000252242.4:n.1439+159C=
ENST00000548409.5:c.561+159C=
ENST00000549511.5:n.646+159C=
ENST00000552629.5:n.1696C=
NM_000424.3:c.1439+159C=	NP_000415.2:n.1439+159C=
NM_000424.4:c.1439+159C= MANE Select	NP_000415.2:n.1439+159C=