Canonical Allele Identifier: CA2260099683

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612297_41612300delinsTAGG , CM000679.2:g.41612297_41612300delinsTAGG	GRCh38
NC_000017.10:g.39768549_39768552delinsTAGG , CM000679.1:g.39768549_39768552delinsTAGG	GRCh37
NC_000017.9:g.37022075_37022078delinsTAGG	NCBI36
NG_008301.1:g.5528_5531delinsCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.389_392delinsCCTA MANE Select	ENSP00000301653.3:p.Ser130=
ENST00000301653.8:c.389_392delinsCCTA	ENSP00000301653.3:p.Ser130=
ENST00000588319.1:n.466_469delinsCCTA
ENST00000593067.1:c.-312-14_-312-11delinsCCTA	ENSP00000467124.1:n.-312-14_-312-11delinsCCTA
NM_005557.3:c.389_392delinsCCTA	NP_005548.2:p.Ser130=
NM_005557.4:c.389_392delinsCCTA MANE Select	NP_005548.2:p.Ser130=