Canonical Allele Identifier: CA1427057067

Gene: KNG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186727258C= , CM000665.2:g.186727258C=	GRCh38
NC_000003.11:g.186445047C= , CM000665.1:g.186445047C=	GRCh37
NC_000003.10:g.187927741C=	NCBI36
NG_016009.1:g.14950C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287611.8:c.586C=	ENSP00000287611.2:p.Arg196=
ENST00000644859.2:c.586C= MANE Select	ENSP00000493985.1:p.Arg196=
ENST00000265023.8:c.586C=	ENSP00000265023.4:p.Arg196=
ENST00000287611.6:c.586C=	ENSP00000287611.2:p.Arg196=
ENST00000447445.1:c.564+1998C=	ENSP00000396025.1:n.564+1998C=
NM_000893.3:c.586C=	NP_000884.1:p.Arg196=
NM_001102416.2:c.586C=	NP_001095886.1:p.Arg196=
NM_001166451.1:c.564+1998C=	NP_001159923.1:n.564+1998C=
NM_000893.4:c.586C=	NP_000884.1:p.Arg196=
NM_001102416.3:c.586C= MANE Select	NP_001095886.1:p.Arg196=
NM_001166451.2:c.564+1998C=	NP_001159923.1:n.564+1998C=