Canonical Allele Identifier: CA2260085697

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584049_41584081delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTT , CM000679.2:g.41584049_41584081delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTT	GRCh38
NC_000017.10:g.39740301_39740333delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTT , CM000679.1:g.39740301_39740333delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTT	GRCh37
NC_000017.9:g.36993827_36993859delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTTT	NCBI36
NG_008624.1:g.7815_7847delinsAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-160_766-128delinsAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG MANE Select	ENSP00000167586.6:n.766-160_766-128delinsAAAAAAAAAAAAGAGAGAGA...
ENST00000167586.6:c.766-160_766-128delinsAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG	ENSP00000167586.6:n.766-160_766-128delinsAAAAAAAAAAAAGAGAGAGA...
ENST00000476662.1:n.216-160_216-128delinsAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG
NM_000526.4:c.766-160_766-128delinsAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG	NP_000517.2:n.766-160_766-128delinsAAAAAAAAAAAAGAGAGAGAGAGAGA...
NM_000526.5:c.766-160_766-128delinsAAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG MANE Select	NP_000517.3:n.766-160_766-128delinsAAAAAAAAAAAAGAGAGAGAGAGAGA...