Canonical Allele Identifier: CA2036540587

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520060A= , CM000674.2:g.52520060A=	GRCh38
NC_000012.11:g.52913844A= , CM000674.1:g.52913844A=	GRCh37
NC_000012.10:g.51200111A=	NCBI36
NG_008297.1:g.5400T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.237T= MANE Select	ENSP00000252242.4:p.Ser79=
ENST00000252242.8:c.237T=	ENSP00000252242.4:p.Ser79=
ENST00000546577.1:c.237T=	ENSP00000449651.1:p.Ser79=
ENST00000549420.1:c.44-137T=	ENSP00000447209.1:n.44-137T=
ENST00000551275.1:c.173-41T=	ENSP00000448041.1:n.173-41T=
ENST00000552629.5:n.335T=
NM_000424.3:c.237T=	NP_000415.2:p.Ser79=
NM_000424.4:c.237T= MANE Select	NP_000415.2:p.Ser79=