Canonical Allele Identifier: CA2260085705
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584049_41584068delinsCAATCTCTCTCTCTCTCTCT , CM000679.2:g.41584049_41584068delinsCAATCTCTCTCTCTCTCTCT GRCh38
NC_000017.10:g.39740301_39740320delinsCAATCTCTCTCTCTCTCTCT , CM000679.1:g.39740301_39740320delinsCAATCTCTCTCTCTCTCTCT GRCh37
NC_000017.9:g.36993827_36993846delinsCAATCTCTCTCTCTCTCTCT NCBI36
NG_008624.1:g.7828_7847delinsAGAGAGAGAGAGAGAGATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-147_766-128delinsAGAGAGAGAGAGAGAGATTG MANE Select ENSP00000167586.6:n.766-147_766-128delinsAGAGAGAGAGAGAGAGATTG...
ENST00000167586.6:c.766-147_766-128delinsAGAGAGAGAGAGAGAGATTG ENSP00000167586.6:n.766-147_766-128delinsAGAGAGAGAGAGAGAGATTG...
ENST00000476662.1:n.216-147_216-128delinsAGAGAGAGAGAGAGAGATTG
NM_000526.4:c.766-147_766-128delinsAGAGAGAGAGAGAGAGATTG NP_000517.2:n.766-147_766-128delinsAGAGAGAGAGAGAGAGATTG
NM_000526.5:c.766-147_766-128delinsAGAGAGAGAGAGAGAGATTG MANE Select NP_000517.3:n.766-147_766-128delinsAGAGAGAGAGAGAGAGATTG