Canonical Allele Identifier: CA2260085698

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584049_41584080delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTT , CM000679.2:g.41584049_41584080delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTT	GRCh38
NC_000017.10:g.39740301_39740332delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTT , CM000679.1:g.39740301_39740332delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTT	GRCh37
NC_000017.9:g.36993827_36993858delinsCAATCTCTCTCTCTCTCTCTCTTTTTTTTTTT	NCBI36
NG_008624.1:g.7816_7847delinsAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-159_766-128delinsAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG MANE Select	ENSP00000167586.6:n.766-159_766-128delinsAAAAAAAAAAAGAGAGAGAG...
ENST00000167586.6:c.766-159_766-128delinsAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG	ENSP00000167586.6:n.766-159_766-128delinsAAAAAAAAAAAGAGAGAGAG...
ENST00000476662.1:n.216-159_216-128delinsAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG
NM_000526.4:c.766-159_766-128delinsAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG	NP_000517.2:n.766-159_766-128delinsAAAAAAAAAAAGAGAGAGAGAGAGAG...
NM_000526.5:c.766-159_766-128delinsAAAAAAAAAAAGAGAGAGAGAGAGAGAGATTG MANE Select	NP_000517.3:n.766-159_766-128delinsAAAAAAAAAAAGAGAGAGAGAGAGAG...