Canonical Allele Identifier: CA2036538996

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516800T= , CM000674.2:g.52516800T=	GRCh38
NC_000012.11:g.52910584T= , CM000674.1:g.52910584T=	GRCh37
NC_000012.10:g.51196851T=	NCBI36
NG_008297.1:g.8660A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1276A= MANE Select	ENSP00000252242.4:p.Lys426=
ENST00000252242.8:c.1276A=	ENSP00000252242.4:p.Lys426=
ENST00000547890.5:n.654A=
ENST00000548409.5:c.398A=
ENST00000549511.5:n.483A=
ENST00000552629.5:n.1374A=
NM_000424.3:c.1276A=	NP_000415.2:p.Lys426=
NM_000424.4:c.1276A= MANE Select	NP_000415.2:p.Lys426=