Canonical Allele Identifier: CA2695225888

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612674dup , CM000679.2:g.41612674dup	GRCh38
NC_000017.10:g.39768926dup , CM000679.1:g.39768926dup	GRCh37
NC_000017.9:g.37022452dup	NCBI36
NG_008301.1:g.5155dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.16dup MANE Select	ENSP00000301653.3:p.Arg6ProfsTer?
ENST00000301653.8:c.16dup	ENSP00000301653.3:p.Arg6ProfsTer?
ENST00000588319.1:n.93dup
ENST00000590990.1:c.16dup	ENSP00000467105.1:p.Arg6ProfsTer?
ENST00000593067.1:c.-313+117dup	ENSP00000467124.1:n.-313+117dup
NM_005557.3:c.16dup	NP_005548.2:p.Arg6ProfsTer?
NM_005557.4:c.16dup MANE Select	NP_005548.2:p.Arg6ProfsTer?