Canonical Allele Identifier: CA2260099880

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612614_41612626delinsCCCGATGCCGCCT , CM000679.2:g.41612614_41612626delinsCCCGATGCCGCCT	GRCh38
NC_000017.10:g.39768866_39768878delinsCCCGATGCCGCCT , CM000679.1:g.39768866_39768878delinsCCCGATGCCGCCT	GRCh37
NC_000017.9:g.37022392_37022404delinsCCCGATGCCGCCT	NCBI36
NG_008301.1:g.5202_5214delinsAGGCGGCATCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.63_75delinsAGGCGGCATCGGG MANE Select	ENSP00000301653.3:p.Gly21=
ENST00000301653.8:c.63_75delinsAGGCGGCATCGGG	ENSP00000301653.3:p.Gly21=
ENST00000588319.1:n.140_152delinsAGGCGGCATCGGG
ENST00000590990.1:c.63_75delinsAGGCGGCATCGGG	ENSP00000467105.1:p.Gly21=
ENST00000593067.1:c.-313+164_-313+176delinsAGGCGGCATCGGG	ENSP00000467124.1:n.-313+164_-313+176delinsAGGCGGCATCGGG
NM_005557.3:c.63_75delinsAGGCGGCATCGGG	NP_005548.2:p.Gly21=
NM_005557.4:c.63_75delinsAGGCGGCATCGGG MANE Select	NP_005548.2:p.Gly21=