Canonical Allele Identifier: CA2260085684
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584034_41584039delinsTCTCTC , CM000679.2:g.41584034_41584039delinsTCTCTC GRCh38
NC_000017.10:g.39740286_39740291delinsTCTCTC , CM000679.1:g.39740286_39740291delinsTCTCTC GRCh37
NC_000017.9:g.36993812_36993817delinsTCTCTC NCBI36
NG_008624.1:g.7857_7862delinsGAGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-118_766-113delinsGAGAGA MANE Select ENSP00000167586.6:n.766-118_766-113delinsGAGAGA
ENST00000167586.6:c.766-118_766-113delinsGAGAGA ENSP00000167586.6:n.766-118_766-113delinsGAGAGA
ENST00000476662.1:n.216-118_216-113delinsGAGAGA
NM_000526.4:c.766-118_766-113delinsGAGAGA NP_000517.2:n.766-118_766-113delinsGAGAGA
NM_000526.5:c.766-118_766-113delinsGAGAGA MANE Select NP_000517.3:n.766-118_766-113delinsGAGAGA