Canonical Allele Identifier: CA2260099946

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612717_41612718delinsGC , CM000679.2:g.41612717_41612718delinsGC	GRCh38
NC_000017.10:g.39768969_39768970delinsGC , CM000679.1:g.39768969_39768970delinsGC	GRCh37
NC_000017.9:g.37022495_37022496delinsGC	NCBI36
NG_008301.1:g.5110_5111delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.-30_-29delinsGC MANE Select	ENSP00000301653.3:n.-30_-29delinsGC
ENST00000301653.8:c.-30_-29delinsGC	ENSP00000301653.3:n.-30_-29delinsGC
ENST00000588319.1:n.48_49delinsGC
ENST00000590990.1:c.-30_-29delinsGC	ENSP00000467105.1:n.-30_-29delinsGC
ENST00000593067.1:c.-313+72_-313+73delinsGC	ENSP00000467124.1:n.-313+72_-313+73delinsGC
NM_005557.3:c.-30_-29delinsGC	NP_005548.2:n.-30_-29delinsGC
NM_005557.4:c.-30_-29delinsGC MANE Select	NP_005548.2:n.-30_-29delinsGC