Canonical Allele Identifier: CA2260099913

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612672C= , CM000679.2:g.41612672C=	GRCh38
NC_000017.10:g.39768924C= , CM000679.1:g.39768924C=	GRCh37
NC_000017.9:g.37022450C=	NCBI36
NG_008301.1:g.5156G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.17G= MANE Select	ENSP00000301653.3:p.Arg6=
ENST00000301653.8:c.17G=	ENSP00000301653.3:p.Arg6=
ENST00000588319.1:n.94G=
ENST00000590990.1:c.17G=	ENSP00000467105.1:p.Arg6=
ENST00000593067.1:c.-313+118G=	ENSP00000467124.1:n.-313+118G=
NM_005557.3:c.17G=	NP_005548.2:p.Arg6=
NM_005557.4:c.17G= MANE Select	NP_005548.2:p.Arg6=