Canonical Allele Identifier: CA2260085712

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584050_41584062delinsAATCTCTCTCTCT , CM000679.2:g.41584050_41584062delinsAATCTCTCTCTCT	GRCh38
NC_000017.10:g.39740302_39740314delinsAATCTCTCTCTCT , CM000679.1:g.39740302_39740314delinsAATCTCTCTCTCT	GRCh37
NC_000017.9:g.36993828_36993840delinsAATCTCTCTCTCT	NCBI36
NG_008624.1:g.7834_7846delinsAGAGAGAGAGATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-141_766-129delinsAGAGAGAGAGATT MANE Select	ENSP00000167586.6:n.766-141_766-129delinsAGAGAGAGAGATT
ENST00000167586.6:c.766-141_766-129delinsAGAGAGAGAGATT	ENSP00000167586.6:n.766-141_766-129delinsAGAGAGAGAGATT
ENST00000476662.1:n.216-141_216-129delinsAGAGAGAGAGATT
NM_000526.4:c.766-141_766-129delinsAGAGAGAGAGATT	NP_000517.2:n.766-141_766-129delinsAGAGAGAGAGATT
NM_000526.5:c.766-141_766-129delinsAGAGAGAGAGATT MANE Select	NP_000517.3:n.766-141_766-129delinsAGAGAGAGAGATT