Canonical Allele Identifier: CA2036538984

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52516777G= , CM000674.2:g.52516777G=	GRCh38
NC_000012.11:g.52910561G= , CM000674.1:g.52910561G=	GRCh37
NC_000012.10:g.51196828G=	NCBI36
NG_008297.1:g.8683C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.1299C= MANE Select	ENSP00000252242.4:p.Ala433=
ENST00000252242.8:c.1299C=	ENSP00000252242.4:p.Ala433=
ENST00000547890.5:n.677C=
ENST00000548409.5:c.421C=
ENST00000549511.5:n.506C=
ENST00000552629.5:n.1397C=
NM_000424.3:c.1299C=	NP_000415.2:p.Ala433=
NM_000424.4:c.1299C= MANE Select	NP_000415.2:p.Ala433=