Canonical Allele Identifier: CA2036540602

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520090C= , CM000674.2:g.52520090C=	GRCh38
NC_000012.11:g.52913874C= , CM000674.1:g.52913874C=	GRCh37
NC_000012.10:g.51200141C=	NCBI36
NG_008297.1:g.5370G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.207G= MANE Select	ENSP00000252242.4:p.Gly69=
ENST00000252242.8:c.207G=	ENSP00000252242.4:p.Gly69=
ENST00000546577.1:c.207G=	ENSP00000449651.1:p.Gly69=
ENST00000549420.1:c.43+164G=	ENSP00000447209.1:n.43+164G=
ENST00000551275.1:c.172+35G=	ENSP00000448041.1:n.172+35G=
ENST00000552629.5:n.305G=
NM_000424.3:c.207G=	NP_000415.2:p.Gly69=
NM_000424.4:c.207G= MANE Select	NP_000415.2:p.Gly69=