Canonical Allele Identifier: CA1427064952

Gene: KNG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186733447T= , CM000665.2:g.186733447T=	GRCh38
NC_000003.11:g.186451236T= , CM000665.1:g.186451236T=	GRCh37
NC_000003.10:g.187933930T=	NCBI36
NG_016009.1:g.21139T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001102416.3:c.930+773T= MANE Select	NP_001095886.1:n.930+773T=
ENST00000644859.2:c.930+773T= MANE Select	ENSP00000493985.1:n.930+773T=
NM_000893.3:c.930+773T=	NP_000884.1:n.930+773T=
NM_000893.4:c.930+773T=	NP_000884.1:n.930+773T=
NM_001102416.2:c.930+773T=	NP_001095886.1:n.930+773T=
NM_001166451.1:c.822+773T=	NP_001159923.1:n.822+773T=
NM_001166451.2:c.822+773T=	NP_001159923.1:n.822+773T=
ENST00000265023.8:c.930+773T=	ENSP00000265023.4:n.930+773T=
ENST00000287611.6:c.930+773T=	ENSP00000287611.2:n.930+773T=
ENST00000287611.8:c.930+773T=	ENSP00000287611.2:n.930+773T=
ENST00000447445.1:c.822+773T=	ENSP00000396025.1:n.822+773T=