Canonical Allele Identifier: CA2036540467

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519824T= , CM000674.2:g.52519824T=	GRCh38
NC_000012.11:g.52913608T= , CM000674.1:g.52913608T=	GRCh37
NC_000012.10:g.51199875T=	NCBI36
NG_008297.1:g.5636A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.473A= MANE Select	ENSP00000252242.4:p.Asp158=
ENST00000252242.8:c.473A=	ENSP00000252242.4:p.Asp158=
ENST00000549420.1:c.143A=	ENSP00000447209.1:p.Asp48=
ENST00000551275.1:c.368A=	ENSP00000448041.1:p.Asp123=
ENST00000552629.5:n.571A=
NM_000424.3:c.473A=	NP_000415.2:p.Asp158=
NM_000424.4:c.473A= MANE Select	NP_000415.2:p.Asp158=