Canonical Allele Identifier: CA2036540676

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520225G= , CM000674.2:g.52520225G=	GRCh38
NC_000012.11:g.52914009G= , CM000674.1:g.52914009G=	GRCh37
NC_000012.10:g.51200276G=	NCBI36
NG_008297.1:g.5235C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.72C= MANE Select	ENSP00000252242.4:p.Thr24=
ENST00000252242.8:c.72C=	ENSP00000252242.4:p.Thr24=
ENST00000546577.1:c.72C=	ENSP00000449651.1:p.Thr24=
ENST00000549420.1:c.43+29C=	ENSP00000447209.1:n.43+29C=
ENST00000551275.1:c.72C=	ENSP00000448041.1:p.Thr24=
ENST00000552629.5:n.170C=
NM_000424.3:c.72C=	NP_000415.2:p.Thr24=
NM_000424.4:c.72C= MANE Select	NP_000415.2:p.Thr24=