Canonical Allele Identifier: CA2260085696

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584049_41584082delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTTT , CM000679.2:g.41584049_41584082delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTTT	GRCh38
NC_000017.10:g.39740301_39740334delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTTT , CM000679.1:g.39740301_39740334delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTTT	GRCh37
NC_000017.9:g.36993827_36993860delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTTT	NCBI36
NG_008624.1:g.7814_7847delinsAAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-161_766-128delinsAAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG MANE Select	ENSP00000167586.6:n.766-161_766-128delinsAAAAAAAAAAAAAGAGAGAG...
ENST00000167586.6:c.766-161_766-128delinsAAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG	ENSP00000167586.6:n.766-161_766-128delinsAAAAAAAAAAAAAGAGAGAG...
ENST00000476662.1:n.216-161_216-128delinsAAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG
NM_000526.4:c.766-161_766-128delinsAAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG	NP_000517.2:n.766-161_766-128delinsAAAAAAAAAAAAAGAGAGAGAGAGAG...
NM_000526.5:c.766-161_766-128delinsAAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG MANE Select	NP_000517.3:n.766-161_766-128delinsAAAAAAAAAAAAAGAGAGAGAGAGAG...