Canonical Allele Identifier: CA2260085710
Gene: KRT14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584049_41584071delinsCAATCTCTCTCTCTCTCTCTCTT , CM000679.2:g.41584049_41584071delinsCAATCTCTCTCTCTCTCTCTCTT GRCh38
NC_000017.10:g.39740301_39740323delinsCAATCTCTCTCTCTCTCTCTCTT , CM000679.1:g.39740301_39740323delinsCAATCTCTCTCTCTCTCTCTCTT GRCh37
NC_000017.9:g.36993827_36993849delinsCAATCTCTCTCTCTCTCTCTCTT NCBI36
NG_008624.1:g.7825_7847delinsAAGAGAGAGAGAGAGAGAGATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.766-150_766-128delinsAAGAGAGAGAGAGAGAGAGATTG MANE Select ENSP00000167586.6:n.766-150_766-128delinsAAGAGAGAGAGAGAGAGAGA...
ENST00000167586.6:c.766-150_766-128delinsAAGAGAGAGAGAGAGAGAGATTG ENSP00000167586.6:n.766-150_766-128delinsAAGAGAGAGAGAGAGAGAGA...
ENST00000476662.1:n.216-150_216-128delinsAAGAGAGAGAGAGAGAGAGATTG
NM_000526.4:c.766-150_766-128delinsAAGAGAGAGAGAGAGAGAGATTG NP_000517.2:n.766-150_766-128delinsAAGAGAGAGAGAGAGAGAGATTG
NM_000526.5:c.766-150_766-128delinsAAGAGAGAGAGAGAGAGAGATTG MANE Select NP_000517.3:n.766-150_766-128delinsAAGAGAGAGAGAGAGAGAGATTG