Canonical Allele Identifier: CA2260085167

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583047_41583048delinsAC , CM000679.2:g.41583047_41583048delinsAC	GRCh38
NC_000017.10:g.39739299_39739300delinsAC , CM000679.1:g.39739299_39739300delinsAC	GRCh37
NC_000017.9:g.36992825_36992826delinsAC	NCBI36
NG_008624.1:g.8848_8849delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.1321+46_1321+47delinsGT MANE Select	ENSP00000167586.6:n.1321+46_1321+47delinsGT
ENST00000167586.6:c.1321+46_1321+47delinsGT	ENSP00000167586.6:n.1321+46_1321+47delinsGT
ENST00000441550.2:n.314_315delinsGT
NM_000526.4:c.1321+46_1321+47delinsGT	NP_000517.2:n.1321+46_1321+47delinsGT
NM_000526.5:c.1321+46_1321+47delinsGT MANE Select	NP_000517.3:n.1321+46_1321+47delinsGT