Canonical Allele Identifier: CA2260099574

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612073_41612089delinsTAAAGTGTAATTGCTAA , CM000679.2:g.41612073_41612089delinsTAAAGTGTAATTGCTAA	GRCh38
NC_000017.10:g.39768325_39768341delinsTAAAGTGTAATTGCTAA , CM000679.1:g.39768325_39768341delinsTAAAGTGTAATTGCTAA	GRCh37
NC_000017.9:g.37021851_37021867delinsTAAAGTGTAATTGCTAA	NCBI36
NG_008301.1:g.5739_5755delinsTTAGCAATTACACTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.531+69_531+85delinsTTAGCAATTACACTTTA MANE Select	ENSP00000301653.3:n.531+69_531+85delinsTTAGCAATTACACTTTA
ENST00000301653.8:c.531+69_531+85delinsTTAGCAATTACACTTTA	ENSP00000301653.3:n.531+69_531+85delinsTTAGCAATTACACTTTA
ENST00000588319.1:n.677_693delinsTTAGCAATTACACTTTA
ENST00000593067.1:c.-184+69_-184+85delinsTTAGCAATTACACTTTA	ENSP00000467124.1:n.-184+69_-184+85delinsTTAGCAATTACACTTTA
NM_005557.3:c.531+69_531+85delinsTTAGCAATTACACTTTA	NP_005548.2:n.531+69_531+85delinsTTAGCAATTACACTTTA
NM_005557.4:c.531+69_531+85delinsTTAGCAATTACACTTTA MANE Select	NP_005548.2:n.531+69_531+85delinsTTAGCAATTACACTTTA