Canonical Allele Identifier: CA2697559864

Gene: KRT14

Linked Data

• ClinVar Variation Id: 2699329
• ClinVar RCV Id: RCV003544568

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583388_41583389insA , CM000679.2:g.41583388_41583389insA	GRCh38
NC_000017.10:g.39739640_39739641insA , CM000679.1:g.39739640_39739641insA	GRCh37
NC_000017.9:g.36993166_36993167insA	NCBI36
NG_008624.1:g.8507_8508insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.1120_1121insT MANE Select	ENSP00000167586.6:p.Gln374LeufsTer?
ENST00000167586.6:c.1120_1121insT	ENSP00000167586.6:p.Gln374LeufsTer?
ENST00000441550.2:n.67_68insT
ENST00000476662.1:n.570_571insT
NM_000526.4:c.1120_1121insT	NP_000517.2:p.Gln374LeufsTer?
NM_000526.5:c.1120_1121insT MANE Select	NP_000517.3:p.Gln374LeufsTer?