Canonical Allele Identifier: CA2260085702

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584049_41584073delinsCAATCTCTCTCTCTCTCTCTCTTTT , CM000679.2:g.41584049_41584073delinsCAATCTCTCTCTCTCTCTCTCTTTT	GRCh38
NC_000017.10:g.39740301_39740325delinsCAATCTCTCTCTCTCTCTCTCTTTT , CM000679.1:g.39740301_39740325delinsCAATCTCTCTCTCTCTCTCTCTTTT	GRCh37
NC_000017.9:g.36993827_36993851delinsCAATCTCTCTCTCTCTCTCTCTTTT	NCBI36
NG_008624.1:g.7823_7847delinsAAAAGAGAGAGAGAGAGAGAGATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-152_766-128delinsAAAAGAGAGAGAGAGAGAGAGATTG MANE Select	ENSP00000167586.6:n.766-152_766-128delinsAAAAGAGAGAGAGAGAGAGA...
ENST00000167586.6:c.766-152_766-128delinsAAAAGAGAGAGAGAGAGAGAGATTG	ENSP00000167586.6:n.766-152_766-128delinsAAAAGAGAGAGAGAGAGAGA...
ENST00000476662.1:n.216-152_216-128delinsAAAAGAGAGAGAGAGAGAGAGATTG
NM_000526.4:c.766-152_766-128delinsAAAAGAGAGAGAGAGAGAGAGATTG	NP_000517.2:n.766-152_766-128delinsAAAAGAGAGAGAGAGAGAGAGATTG
NM_000526.5:c.766-152_766-128delinsAAAAGAGAGAGAGAGAGAGAGATTG MANE Select	NP_000517.3:n.766-152_766-128delinsAAAAGAGAGAGAGAGAGAGAGATTG