Canonical Allele Identifier: CA2036540702

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520270G= , CM000674.2:g.52520270G=	GRCh38
NC_000012.11:g.52914054G= , CM000674.1:g.52914054G=	GRCh37
NC_000012.10:g.51200321G=	NCBI36
NG_008297.1:g.5190C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.27C= MANE Select	ENSP00000252242.4:p.Phe9=
ENST00000252242.8:c.27C=	ENSP00000252242.4:p.Phe9=
ENST00000546577.1:c.27C=	ENSP00000449651.1:p.Phe9=
ENST00000549420.1:c.27C=	ENSP00000447209.1:p.Phe9=
ENST00000551275.1:c.27C=	ENSP00000448041.1:p.Phe9=
ENST00000552629.5:n.125C=
NM_000424.3:c.27C=	NP_000415.2:p.Phe9=
NM_000424.4:c.27C= MANE Select	NP_000415.2:p.Phe9=