Canonical Allele Identifier: CA2036538994

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516796T= , CM000674.2:g.52516796T=	GRCh38
NC_000012.11:g.52910580T= , CM000674.1:g.52910580T=	GRCh37
NC_000012.10:g.51196847T=	NCBI36
NG_008297.1:g.8664A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1280A= MANE Select	ENSP00000252242.4:p.Asp427=
ENST00000252242.8:c.1280A=	ENSP00000252242.4:p.Asp427=
ENST00000547890.5:n.658A=
ENST00000548409.5:c.402A=
ENST00000549511.5:n.487A=
ENST00000552629.5:n.1378A=
NM_000424.3:c.1280A=	NP_000415.2:p.Asp427=
NM_000424.4:c.1280A= MANE Select	NP_000415.2:p.Asp427=