Canonical Allele Identifier: CA2260085711

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584049_41584069delinsCAATCTCTCTCTCTCTCTCTC , CM000679.2:g.41584049_41584069delinsCAATCTCTCTCTCTCTCTCTC	GRCh38
NC_000017.10:g.39740301_39740321delinsCAATCTCTCTCTCTCTCTCTC , CM000679.1:g.39740301_39740321delinsCAATCTCTCTCTCTCTCTCTC	GRCh37
NC_000017.9:g.36993827_36993847delinsCAATCTCTCTCTCTCTCTCTC	NCBI36
NG_008624.1:g.7827_7847delinsGAGAGAGAGAGAGAGAGATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-148_766-128delinsGAGAGAGAGAGAGAGAGATTG MANE Select	ENSP00000167586.6:n.766-148_766-128delinsGAGAGAGAGAGAGAGAGATT...
ENST00000167586.6:c.766-148_766-128delinsGAGAGAGAGAGAGAGAGATTG	ENSP00000167586.6:n.766-148_766-128delinsGAGAGAGAGAGAGAGAGATT...
ENST00000476662.1:n.216-148_216-128delinsGAGAGAGAGAGAGAGAGATTG
NM_000526.4:c.766-148_766-128delinsGAGAGAGAGAGAGAGAGATTG	NP_000517.2:n.766-148_766-128delinsGAGAGAGAGAGAGAGAGATTG
NM_000526.5:c.766-148_766-128delinsGAGAGAGAGAGAGAGAGATTG MANE Select	NP_000517.3:n.766-148_766-128delinsGAGAGAGAGAGAGAGAGATTG