Canonical Allele Identifier: CA2260085572

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583799C= , CM000679.2:g.41583799C=	GRCh38
NC_000017.10:g.39740051C= , CM000679.1:g.39740051C=	GRCh37
NC_000017.9:g.36993577C=	NCBI36
NG_008624.1:g.8097G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.888G= MANE Select	ENSP00000167586.6:p.Glu296=
ENST00000167586.6:c.888G=	ENSP00000167586.6:p.Glu296=
ENST00000476662.1:n.338G=
NM_000526.4:c.888G=	NP_000517.2:p.Glu296=
NM_000526.5:c.888G= MANE Select	NP_000517.3:p.Glu296=