Canonical Allele Identifier: CA2036540557

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519998C= , CM000674.2:g.52519998C=	GRCh38
NC_000012.11:g.52913782C= , CM000674.1:g.52913782C=	GRCh37
NC_000012.10:g.51200049C=	NCBI36
NG_008297.1:g.5462G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.299G= MANE Select	ENSP00000252242.4:p.Gly100=
ENST00000252242.8:c.299G=	ENSP00000252242.4:p.Gly100=
ENST00000546577.1:c.299G=	ENSP00000449651.1:p.Gly100=
ENST00000549420.1:c.44-75G=	ENSP00000447209.1:n.44-75G=
ENST00000551275.1:c.194G=	ENSP00000448041.1:p.Gly65=
ENST00000552629.5:n.397G=
NM_000424.3:c.299G=	NP_000415.2:p.Gly100=
NM_000424.4:c.299G= MANE Select	NP_000415.2:p.Gly100=