Canonical Allele Identifier: CA2260085461

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583574C= , CM000679.2:g.41583574C=	GRCh38
NC_000017.10:g.39739826C= , CM000679.1:g.39739826C=	GRCh37
NC_000017.9:g.36993352C=	NCBI36
NG_008624.1:g.8322G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.1030G= MANE Select	ENSP00000167586.6:p.Glu344=
ENST00000167586.6:c.1030G=	ENSP00000167586.6:p.Glu344=
ENST00000476662.1:n.480G=
NM_000526.4:c.1030G=	NP_000517.2:p.Glu344=
NM_000526.5:c.1030G= MANE Select	NP_000517.3:p.Glu344=