Canonical Allele Identifier: CA2036540536

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519968C= , CM000674.2:g.52519968C=	GRCh38
NC_000012.11:g.52913752C= , CM000674.1:g.52913752C=	GRCh37
NC_000012.10:g.51200019C=	NCBI36
NG_008297.1:g.5492G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.329G= MANE Select	ENSP00000252242.4:p.Gly110=
ENST00000252242.8:c.329G=	ENSP00000252242.4:p.Gly110=
ENST00000546577.1:c.329G=	ENSP00000449651.1:p.Gly110=
ENST00000549420.1:c.44-45G=	ENSP00000447209.1:n.44-45G=
ENST00000551275.1:c.224G=	ENSP00000448041.1:p.Gly75=
ENST00000552629.5:n.427G=
NM_000424.3:c.329G=	NP_000415.2:p.Gly110=
NM_000424.4:c.329G= MANE Select	NP_000415.2:p.Gly110=