Canonical Allele Identifier: CA2260085709

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584049_41584066delinsCAATCTCTCTCTCTCTCT , CM000679.2:g.41584049_41584066delinsCAATCTCTCTCTCTCTCT	GRCh38
NC_000017.10:g.39740301_39740318delinsCAATCTCTCTCTCTCTCT , CM000679.1:g.39740301_39740318delinsCAATCTCTCTCTCTCTCT	GRCh37
NC_000017.9:g.36993827_36993844delinsCAATCTCTCTCTCTCTCT	NCBI36
NG_008624.1:g.7830_7847delinsAGAGAGAGAGAGAGATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-145_766-128delinsAGAGAGAGAGAGAGATTG MANE Select	ENSP00000167586.6:n.766-145_766-128delinsAGAGAGAGAGAGAGATTG
ENST00000167586.6:c.766-145_766-128delinsAGAGAGAGAGAGAGATTG	ENSP00000167586.6:n.766-145_766-128delinsAGAGAGAGAGAGAGATTG
ENST00000476662.1:n.216-145_216-128delinsAGAGAGAGAGAGAGATTG
NM_000526.4:c.766-145_766-128delinsAGAGAGAGAGAGAGATTG	NP_000517.2:n.766-145_766-128delinsAGAGAGAGAGAGAGATTG
NM_000526.5:c.766-145_766-128delinsAGAGAGAGAGAGAGATTG MANE Select	NP_000517.3:n.766-145_766-128delinsAGAGAGAGAGAGAGATTG