Canonical Allele Identifier: CA2036538816

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516473G= , CM000674.2:g.52516473G=	GRCh38
NC_000012.11:g.52910257G= , CM000674.1:g.52910257G=	GRCh37
NC_000012.10:g.51196524G=	NCBI36
NG_008297.1:g.8987C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1439+164C= MANE Select	ENSP00000252242.4:n.1439+164C=
ENST00000252242.8:c.1439+164C=	ENSP00000252242.4:n.1439+164C=
ENST00000548409.5:c.561+164C=
ENST00000549511.5:n.646+164C=
ENST00000552629.5:n.1701C=
NM_000424.3:c.1439+164C=	NP_000415.2:n.1439+164C=
NM_000424.4:c.1439+164C= MANE Select	NP_000415.2:n.1439+164C=