Canonical Allele Identifier: CA2260099870

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612601G= , CM000679.2:g.41612601G=	GRCh38
NC_000017.10:g.39768853G= , CM000679.1:g.39768853G=	GRCh37
NC_000017.9:g.37022379G=	NCBI36
NG_008301.1:g.5227C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.88C= MANE Select	ENSP00000301653.3:p.Arg30=
ENST00000301653.8:c.88C=	ENSP00000301653.3:p.Arg30=
ENST00000588319.1:n.165C=
ENST00000590990.1:c.88C=	ENSP00000467105.1:p.Arg30=
ENST00000593067.1:c.-313+189C=	ENSP00000467124.1:n.-313+189C=
NM_005557.3:c.88C=	NP_005548.2:p.Arg30=
NM_005557.4:c.88C= MANE Select	NP_005548.2:p.Arg30=