Canonical Allele Identifier: CA2260085858

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584242C= , CM000679.2:g.41584242C=	GRCh38
NC_000017.10:g.39740494C= , CM000679.1:g.39740494C=	GRCh37
NC_000017.9:g.36994020C=	NCBI36
NG_008624.1:g.7654G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.765+15G= MANE Select	ENSP00000167586.6:n.765+15G=
ENST00000167586.6:c.765+15G=	ENSP00000167586.6:n.765+15G=
ENST00000476662.1:n.215+15G=
NM_000526.4:c.765+15G=	NP_000517.2:n.765+15G=
NM_000526.5:c.765+15G= MANE Select	NP_000517.3:n.765+15G=