Canonical Allele Identifier: CA2036540484

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519853A= , CM000674.2:g.52519853A=	GRCh38
NC_000012.11:g.52913637A= , CM000674.1:g.52913637A=	GRCh37
NC_000012.10:g.51199904A=	NCBI36
NG_008297.1:g.5607T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.444T= MANE Select	ENSP00000252242.4:p.Ser148=
ENST00000252242.8:c.444T=	ENSP00000252242.4:p.Ser148=
ENST00000549420.1:c.114T=	ENSP00000447209.1:p.Ser38=
ENST00000551275.1:c.339T=	ENSP00000448041.1:p.Ser113=
ENST00000552629.5:n.542T=
NM_000424.3:c.444T=	NP_000415.2:p.Ser148=
NM_000424.4:c.444T= MANE Select	NP_000415.2:p.Ser148=