Canonical Allele Identifier: CA2260099830

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612540_41612541delinsAG , CM000679.2:g.41612540_41612541delinsAG	GRCh38
NC_000017.10:g.39768792_39768793delinsAG , CM000679.1:g.39768792_39768793delinsAG	GRCh37
NC_000017.9:g.37022318_37022319delinsAG	NCBI36
NG_008301.1:g.5287_5288delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.148_149delinsCT MANE Select	ENSP00000301653.3:p.Leu50=
ENST00000301653.8:c.148_149delinsCT	ENSP00000301653.3:p.Leu50=
ENST00000588319.1:n.225_226delinsCT
ENST00000593067.1:c.-313+249_-313+250delinsCT	ENSP00000467124.1:n.-313+249_-313+250delinsCT
NM_005557.3:c.148_149delinsCT	NP_005548.2:p.Leu50=
NM_005557.4:c.148_149delinsCT MANE Select	NP_005548.2:p.Leu50=