Canonical Allele Identifier: CA2260085714

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584050_41584064delinsAATCTCTCTCTCTCT , CM000679.2:g.41584050_41584064delinsAATCTCTCTCTCTCT	GRCh38
NC_000017.10:g.39740302_39740316delinsAATCTCTCTCTCTCT , CM000679.1:g.39740302_39740316delinsAATCTCTCTCTCTCT	GRCh37
NC_000017.9:g.36993828_36993842delinsAATCTCTCTCTCTCT	NCBI36
NG_008624.1:g.7832_7846delinsAGAGAGAGAGAGATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-143_766-129delinsAGAGAGAGAGAGATT MANE Select	ENSP00000167586.6:n.766-143_766-129delinsAGAGAGAGAGAGATT
ENST00000167586.6:c.766-143_766-129delinsAGAGAGAGAGAGATT	ENSP00000167586.6:n.766-143_766-129delinsAGAGAGAGAGAGATT
ENST00000476662.1:n.216-143_216-129delinsAGAGAGAGAGAGATT
NM_000526.4:c.766-143_766-129delinsAGAGAGAGAGAGATT	NP_000517.2:n.766-143_766-129delinsAGAGAGAGAGAGATT
NM_000526.5:c.766-143_766-129delinsAGAGAGAGAGAGATT MANE Select	NP_000517.3:n.766-143_766-129delinsAGAGAGAGAGAGATT