Canonical Allele Identifier: CA2260085932

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584419A= , CM000679.2:g.41584419A=	GRCh38
NC_000017.10:g.39740671A= , CM000679.1:g.39740671A=	GRCh37
NC_000017.9:g.36994197A=	NCBI36
NG_008624.1:g.7477T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.609-6T= MANE Select	ENSP00000167586.6:n.609-6T=
ENST00000167586.6:c.609-6T=	ENSP00000167586.6:n.609-6T=
ENST00000476662.1:n.53T=
NM_000526.4:c.609-6T=	NP_000517.2:n.609-6T=
NM_000526.5:c.609-6T= MANE Select	NP_000517.3:n.609-6T=