Canonical Allele Identifier: CA2260086019

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584609_41584610delinsCA , CM000679.2:g.41584609_41584610delinsCA	GRCh38
NC_000017.10:g.39740861_39740862delinsCA , CM000679.1:g.39740861_39740862delinsCA	GRCh37
NC_000017.9:g.36994387_36994388delinsCA	NCBI36
NG_008624.1:g.7286_7287delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.609-197_609-196delinsTG MANE Select	ENSP00000167586.6:n.609-197_609-196delinsTG
ENST00000167586.6:c.609-197_609-196delinsTG	ENSP00000167586.6:n.609-197_609-196delinsTG
NM_000526.4:c.609-197_609-196delinsTG	NP_000517.2:n.609-197_609-196delinsTG
NM_000526.5:c.609-197_609-196delinsTG MANE Select	NP_000517.3:n.609-197_609-196delinsTG