Canonical Allele Identifier: CA2036538782

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516414G= , CM000674.2:g.52516414G=	GRCh38
NC_000012.11:g.52910198G= , CM000674.1:g.52910198G=	GRCh37
NC_000012.10:g.51196465G=	NCBI36
NG_008297.1:g.9046C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1439+223C= MANE Select	ENSP00000252242.4:n.1439+223C=
ENST00000252242.8:c.1439+223C=	ENSP00000252242.4:n.1439+223C=
ENST00000548409.5:c.561+223C=
ENST00000549511.5:n.646+223C=
ENST00000552629.5:n.1760C=
NM_000424.3:c.1439+223C=	NP_000415.2:n.1439+223C=
NM_000424.4:c.1439+223C= MANE Select	NP_000415.2:n.1439+223C=