Canonical Allele Identifier: CA2036540487

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52519866G= , CM000674.2:g.52519866G=	GRCh38
NC_000012.11:g.52913650G= , CM000674.1:g.52913650G=	GRCh37
NC_000012.10:g.51199917G=	NCBI36
NG_008297.1:g.5594C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.431C= MANE Select	ENSP00000252242.4:p.Thr144=
ENST00000252242.8:c.431C=	ENSP00000252242.4:p.Thr144=
ENST00000549420.1:c.101C=	ENSP00000447209.1:p.Thr34=
ENST00000551275.1:c.326C=	ENSP00000448041.1:p.Thr109=
ENST00000552629.5:n.529C=
NM_000424.3:c.431C=	NP_000415.2:p.Thr144=
NM_000424.4:c.431C= MANE Select	NP_000415.2:p.Thr144=