Canonical Allele Identifier: CA2260085703

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584049_41584064delinsCAATCTCTCTCTCTCT , CM000679.2:g.41584049_41584064delinsCAATCTCTCTCTCTCT	GRCh38
NC_000017.10:g.39740301_39740316delinsCAATCTCTCTCTCTCT , CM000679.1:g.39740301_39740316delinsCAATCTCTCTCTCTCT	GRCh37
NC_000017.9:g.36993827_36993842delinsCAATCTCTCTCTCTCT	NCBI36
NG_008624.1:g.7832_7847delinsAGAGAGAGAGAGATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-143_766-128delinsAGAGAGAGAGAGATTG MANE Select	ENSP00000167586.6:n.766-143_766-128delinsAGAGAGAGAGAGATTG
ENST00000167586.6:c.766-143_766-128delinsAGAGAGAGAGAGATTG	ENSP00000167586.6:n.766-143_766-128delinsAGAGAGAGAGAGATTG
ENST00000476662.1:n.216-143_216-128delinsAGAGAGAGAGAGATTG
NM_000526.4:c.766-143_766-128delinsAGAGAGAGAGAGATTG	NP_000517.2:n.766-143_766-128delinsAGAGAGAGAGAGATTG
NM_000526.5:c.766-143_766-128delinsAGAGAGAGAGAGATTG MANE Select	NP_000517.3:n.766-143_766-128delinsAGAGAGAGAGAGATTG