Canonical Allele Identifier: CA2260099613

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612153C= , CM000679.2:g.41612153C=	GRCh38
NC_000017.10:g.39768405C= , CM000679.1:g.39768405C=	GRCh37
NC_000017.9:g.37021931C=	NCBI36
NG_008301.1:g.5675G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.531+5G= MANE Select	ENSP00000301653.3:n.531+5G=
ENST00000301653.8:c.531+5G=	ENSP00000301653.3:n.531+5G=
ENST00000588319.1:n.613G=
ENST00000593067.1:c.-184+5G=	ENSP00000467124.1:n.-184+5G=
NM_005557.3:c.531+5G=	NP_005548.2:n.531+5G=
NM_005557.4:c.531+5G= MANE Select	NP_005548.2:n.531+5G=