Canonical Allele Identifier: CA2260085728

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584052_41584069delinsTCTCTCTCTCTCTCTCTC , CM000679.2:g.41584052_41584069delinsTCTCTCTCTCTCTCTCTC	GRCh38
NC_000017.10:g.39740304_39740321delinsTCTCTCTCTCTCTCTCTC , CM000679.1:g.39740304_39740321delinsTCTCTCTCTCTCTCTCTC	GRCh37
NC_000017.9:g.36993830_36993847delinsTCTCTCTCTCTCTCTCTC	NCBI36
NG_008624.1:g.7827_7844delinsGAGAGAGAGAGAGAGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-148_766-131delinsGAGAGAGAGAGAGAGAGA MANE Select	ENSP00000167586.6:n.766-148_766-131delinsGAGAGAGAGAGAGAGAGA
ENST00000167586.6:c.766-148_766-131delinsGAGAGAGAGAGAGAGAGA	ENSP00000167586.6:n.766-148_766-131delinsGAGAGAGAGAGAGAGAGA
ENST00000476662.1:n.216-148_216-131delinsGAGAGAGAGAGAGAGAGA
NM_000526.4:c.766-148_766-131delinsGAGAGAGAGAGAGAGAGA	NP_000517.2:n.766-148_766-131delinsGAGAGAGAGAGAGAGAGA
NM_000526.5:c.766-148_766-131delinsGAGAGAGAGAGAGAGAGA MANE Select	NP_000517.3:n.766-148_766-131delinsGAGAGAGAGAGAGAGAGA