Canonical Allele Identifier: CA2260085726

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584052_41584065delinsTCTCTCTCTCTCTC , CM000679.2:g.41584052_41584065delinsTCTCTCTCTCTCTC	GRCh38
NC_000017.10:g.39740304_39740317delinsTCTCTCTCTCTCTC , CM000679.1:g.39740304_39740317delinsTCTCTCTCTCTCTC	GRCh37
NC_000017.9:g.36993830_36993843delinsTCTCTCTCTCTCTC	NCBI36
NG_008624.1:g.7831_7844delinsGAGAGAGAGAGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-144_766-131delinsGAGAGAGAGAGAGA MANE Select	ENSP00000167586.6:n.766-144_766-131delinsGAGAGAGAGAGAGA
ENST00000167586.6:c.766-144_766-131delinsGAGAGAGAGAGAGA	ENSP00000167586.6:n.766-144_766-131delinsGAGAGAGAGAGAGA
ENST00000476662.1:n.216-144_216-131delinsGAGAGAGAGAGAGA
NM_000526.4:c.766-144_766-131delinsGAGAGAGAGAGAGA	NP_000517.2:n.766-144_766-131delinsGAGAGAGAGAGAGA
NM_000526.5:c.766-144_766-131delinsGAGAGAGAGAGAGA MANE Select	NP_000517.3:n.766-144_766-131delinsGAGAGAGAGAGAGA