Canonical Allele Identifier: CA2260085686

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584035_41584051delinsCTCTCTCTCTCTCTCAA , CM000679.2:g.41584035_41584051delinsCTCTCTCTCTCTCTCAA	GRCh38
NC_000017.10:g.39740287_39740303delinsCTCTCTCTCTCTCTCAA , CM000679.1:g.39740287_39740303delinsCTCTCTCTCTCTCTCAA	GRCh37
NC_000017.9:g.36993813_36993829delinsCTCTCTCTCTCTCTCAA	NCBI36
NG_008624.1:g.7845_7861delinsTTGAGAGAGAGAGAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-130_766-114delinsTTGAGAGAGAGAGAGAG MANE Select	ENSP00000167586.6:n.766-130_766-114delinsTTGAGAGAGAGAGAGAG
ENST00000167586.6:c.766-130_766-114delinsTTGAGAGAGAGAGAGAG	ENSP00000167586.6:n.766-130_766-114delinsTTGAGAGAGAGAGAGAG
ENST00000476662.1:n.216-130_216-114delinsTTGAGAGAGAGAGAGAG
NM_000526.4:c.766-130_766-114delinsTTGAGAGAGAGAGAGAG	NP_000517.2:n.766-130_766-114delinsTTGAGAGAGAGAGAGAG
NM_000526.5:c.766-130_766-114delinsTTGAGAGAGAGAGAGAG MANE Select	NP_000517.3:n.766-130_766-114delinsTTGAGAGAGAGAGAGAG