Canonical Allele Identifier: CA2260085695

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584048_41584069delinsTCAATCTCTCTCTCTCTCTCTC , CM000679.2:g.41584048_41584069delinsTCAATCTCTCTCTCTCTCTCTC	GRCh38
NC_000017.10:g.39740300_39740321delinsTCAATCTCTCTCTCTCTCTCTC , CM000679.1:g.39740300_39740321delinsTCAATCTCTCTCTCTCTCTCTC	GRCh37
NC_000017.9:g.36993826_36993847delinsTCAATCTCTCTCTCTCTCTCTC	NCBI36
NG_008624.1:g.7827_7848delinsGAGAGAGAGAGAGAGAGATTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-148_766-127delinsGAGAGAGAGAGAGAGAGATTGA MANE Select	ENSP00000167586.6:n.766-148_766-127delinsGAGAGAGAGAGAGAGAGATT...
ENST00000167586.6:c.766-148_766-127delinsGAGAGAGAGAGAGAGAGATTGA	ENSP00000167586.6:n.766-148_766-127delinsGAGAGAGAGAGAGAGAGATT...
ENST00000476662.1:n.216-148_216-127delinsGAGAGAGAGAGAGAGAGATTGA
NM_000526.4:c.766-148_766-127delinsGAGAGAGAGAGAGAGAGATTGA	NP_000517.2:n.766-148_766-127delinsGAGAGAGAGAGAGAGAGATTGA
NM_000526.5:c.766-148_766-127delinsGAGAGAGAGAGAGAGAGATTGA MANE Select	NP_000517.3:n.766-148_766-127delinsGAGAGAGAGAGAGAGAGATTGA