Canonical Allele Identifier: CA2260099588

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612108C= , CM000679.2:g.41612108C=	GRCh38
NC_000017.10:g.39768360C= , CM000679.1:g.39768360C=	GRCh37
NC_000017.9:g.37021886C=	NCBI36
NG_008301.1:g.5720G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.531+50G= MANE Select	ENSP00000301653.3:n.531+50G=
ENST00000301653.8:c.531+50G=	ENSP00000301653.3:n.531+50G=
ENST00000588319.1:n.658G=
ENST00000593067.1:c.-184+50G=	ENSP00000467124.1:n.-184+50G=
NM_005557.3:c.531+50G=	NP_005548.2:n.531+50G=
NM_005557.4:c.531+50G= MANE Select	NP_005548.2:n.531+50G=