Canonical Allele Identifier: CA1427072065

Gene: KNG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186742140C= , CM000665.2:g.186742140C=	GRCh38
NC_000003.11:g.186459929C= , CM000665.1:g.186459929C=	GRCh37
NC_000003.10:g.187942623C=	NCBI36
NG_016009.1:g.29832C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287611.8:c.1203+541C=	ENSP00000287611.2:n.1203+541C=
ENST00000644859.2:c.1744C= MANE Select	ENSP00000493985.1:p.Gln582=
ENST00000265023.8:c.1744C=	ENSP00000265023.4:p.Gln582=
ENST00000287611.6:c.1203+541C=	ENSP00000287611.2:n.1203+541C=
ENST00000447445.1:c.1095+541C=	ENSP00000396025.1:n.1095+541C=
NM_000893.3:c.1203+541C=	NP_000884.1:n.1203+541C=
NM_001102416.2:c.1744C=	NP_001095886.1:p.Gln582=
NM_001166451.1:c.1095+541C=	NP_001159923.1:n.1095+541C=
NM_000893.4:c.1203+541C=	NP_000884.1:n.1203+541C=
NM_001102416.3:c.1744C= MANE Select	NP_001095886.1:p.Gln582=
NM_001166451.2:c.1095+541C=	NP_001159923.1:n.1095+541C=