Canonical Allele Identifier: CA2260099867

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612595_41612616delinsAGATGCGGCTGGAGCCGCCCCC , CM000679.2:g.41612595_41612616delinsAGATGCGGCTGGAGCCGCCCCC	GRCh38
NC_000017.10:g.39768847_39768868delinsAGATGCGGCTGGAGCCGCCCCC , CM000679.1:g.39768847_39768868delinsAGATGCGGCTGGAGCCGCCCCC	GRCh37
NC_000017.9:g.37022373_37022394delinsAGATGCGGCTGGAGCCGCCCCC	NCBI36
NG_008301.1:g.5212_5233delinsGGGGGCGGCTCCAGCCGCATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.73_94delinsGGGGGCGGCTCCAGCCGCATCT MANE Select	ENSP00000301653.3:p.Gly25=
ENST00000301653.8:c.73_94delinsGGGGGCGGCTCCAGCCGCATCT	ENSP00000301653.3:p.Gly25=
ENST00000588319.1:n.150_171delinsGGGGGCGGCTCCAGCCGCATCT
ENST00000590990.1:c.73_94delinsGGGGGCGGCTCCAGCCGCATCT	ENSP00000467105.1:p.Gly25=
ENST00000593067.1:c.-313+174_-313+195delinsGGGGGCGGCTCCAGCCGCATCT	ENSP00000467124.1:n.-313+174_-313+195delinsGGGGGCGGCTCCAGCCGC...
NM_005557.3:c.73_94delinsGGGGGCGGCTCCAGCCGCATCT	NP_005548.2:p.Gly25=
NM_005557.4:c.73_94delinsGGGGGCGGCTCCAGCCGCATCT MANE Select	NP_005548.2:p.Gly25=