Canonical Allele Identifier: CA2260085334

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583298A= , CM000679.2:g.41583298A=	GRCh38
NC_000017.10:g.39739550A= , CM000679.1:g.39739550A=	GRCh37
NC_000017.9:g.36993076A=	NCBI36
NG_008624.1:g.8598T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.1211T= MANE Select	ENSP00000167586.6:p.Val404=
ENST00000167586.6:c.1211T=	ENSP00000167586.6:p.Val404=
ENST00000441550.2:n.158T=
ENST00000476662.1:n.661T=
NM_000526.4:c.1211T=	NP_000517.2:p.Val404=
NM_000526.5:c.1211T= MANE Select	NP_000517.3:p.Val404=