Canonical Allele Identifier: CA2260086041

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584652_41584653delinsGC , CM000679.2:g.41584652_41584653delinsGC	GRCh38
NC_000017.10:g.39740904_39740905delinsGC , CM000679.1:g.39740904_39740905delinsGC	GRCh37
NC_000017.9:g.36994430_36994431delinsGC	NCBI36
NG_008624.1:g.7243_7244delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.609-240_609-239delinsGC MANE Select	ENSP00000167586.6:n.609-240_609-239delinsGC
ENST00000167586.6:c.609-240_609-239delinsGC	ENSP00000167586.6:n.609-240_609-239delinsGC
NM_000526.4:c.609-240_609-239delinsGC	NP_000517.2:n.609-240_609-239delinsGC
NM_000526.5:c.609-240_609-239delinsGC MANE Select	NP_000517.3:n.609-240_609-239delinsGC