Canonical Allele Identifier: CA2260085490

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583625C= , CM000679.2:g.41583625C=	GRCh38
NC_000017.10:g.39739877C= , CM000679.1:g.39739877C=	GRCh37
NC_000017.9:g.36993403C=	NCBI36
NG_008624.1:g.8271G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.979G= MANE Select	ENSP00000167586.6:p.Gly327=
ENST00000167586.6:c.979G=	ENSP00000167586.6:p.Gly327=
ENST00000476662.1:n.429G=
NM_000526.4:c.979G=	NP_000517.2:p.Gly327=
NM_000526.5:c.979G= MANE Select	NP_000517.3:p.Gly327=