Canonical Allele Identifier: CA2260099671

Gene: KRT16

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41612273T= , CM000679.2:g.41612273T=	GRCh38
NC_000017.10:g.39768525T= , CM000679.1:g.39768525T=	GRCh37
NC_000017.9:g.37022051T=	NCBI36
NG_008301.1:g.5555A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301653.9:c.416A= MANE Select	ENSP00000301653.3:p.Glu139=
ENST00000301653.8:c.416A=	ENSP00000301653.3:p.Glu139=
ENST00000588319.1:n.493A=
ENST00000593067.1:c.-299A=	ENSP00000467124.1:n.-299A=
NM_005557.3:c.416A=	NP_005548.2:p.Glu139=
NM_005557.4:c.416A= MANE Select	NP_005548.2:p.Glu139=