Canonical Allele Identifier: CA2260085683

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584033_41584051delinsTTCTCTCTCTCTCTCTCAA , CM000679.2:g.41584033_41584051delinsTTCTCTCTCTCTCTCTCAA	GRCh38
NC_000017.10:g.39740285_39740303delinsTTCTCTCTCTCTCTCTCAA , CM000679.1:g.39740285_39740303delinsTTCTCTCTCTCTCTCTCAA	GRCh37
NC_000017.9:g.36993811_36993829delinsTTCTCTCTCTCTCTCTCAA	NCBI36
NG_008624.1:g.7845_7863delinsTTGAGAGAGAGAGAGAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-130_766-112delinsTTGAGAGAGAGAGAGAGAA MANE Select	ENSP00000167586.6:n.766-130_766-112delinsTTGAGAGAGAGAGAGAGAA
ENST00000167586.6:c.766-130_766-112delinsTTGAGAGAGAGAGAGAGAA	ENSP00000167586.6:n.766-130_766-112delinsTTGAGAGAGAGAGAGAGAA
ENST00000476662.1:n.216-130_216-112delinsTTGAGAGAGAGAGAGAGAA
NM_000526.4:c.766-130_766-112delinsTTGAGAGAGAGAGAGAGAA	NP_000517.2:n.766-130_766-112delinsTTGAGAGAGAGAGAGAGAA
NM_000526.5:c.766-130_766-112delinsTTGAGAGAGAGAGAGAGAA MANE Select	NP_000517.3:n.766-130_766-112delinsTTGAGAGAGAGAGAGAGAA