Canonical Allele Identifier: CA2036540586

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520057A= , CM000674.2:g.52520057A=	GRCh38
NC_000012.11:g.52913841A= , CM000674.1:g.52913841A=	GRCh37
NC_000012.10:g.51200108A=	NCBI36
NG_008297.1:g.5403T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.240T= MANE Select	ENSP00000252242.4:p.Gly80=
ENST00000252242.8:c.240T=	ENSP00000252242.4:p.Gly80=
ENST00000546577.1:c.240T=	ENSP00000449651.1:p.Gly80=
ENST00000549420.1:c.44-134T=	ENSP00000447209.1:n.44-134T=
ENST00000551275.1:c.173-38T=	ENSP00000448041.1:n.173-38T=
ENST00000552629.5:n.338T=
NM_000424.3:c.240T=	NP_000415.2:p.Gly80=
NM_000424.4:c.240T= MANE Select	NP_000415.2:p.Gly80=