Canonical Allele Identifier: CA2036540486

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519863A= , CM000674.2:g.52519863A=	GRCh38
NC_000012.11:g.52913647A= , CM000674.1:g.52913647A=	GRCh37
NC_000012.10:g.51199914A=	NCBI36
NG_008297.1:g.5597T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.434T= MANE Select	ENSP00000252242.4:p.Val145=
ENST00000252242.8:c.434T=	ENSP00000252242.4:p.Val145=
ENST00000549420.1:c.104T=	ENSP00000447209.1:p.Val35=
ENST00000551275.1:c.329T=	ENSP00000448041.1:p.Val110=
ENST00000552629.5:n.532T=
NM_000424.3:c.434T=	NP_000415.2:p.Val145=
NM_000424.4:c.434T= MANE Select	NP_000415.2:p.Val145=