Canonical Allele Identifier: CA1427066342

Gene: KNG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186735096A= , CM000665.2:g.186735096A=	GRCh38
NC_000003.11:g.186452885A= , CM000665.1:g.186452885A=	GRCh37
NC_000003.10:g.187935579A=	NCBI36
NG_016009.1:g.22788A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287611.8:c.930+2422A=	ENSP00000287611.2:n.930+2422A=
ENST00000644859.2:c.930+2422A= MANE Select	ENSP00000493985.1:n.930+2422A=
ENST00000265023.8:c.930+2422A=	ENSP00000265023.4:n.930+2422A=
ENST00000287611.6:c.930+2422A=	ENSP00000287611.2:n.930+2422A=
ENST00000447445.1:c.822+2422A=	ENSP00000396025.1:n.822+2422A=
NM_000893.3:c.930+2422A=	NP_000884.1:n.930+2422A=
NM_001102416.2:c.930+2422A=	NP_001095886.1:n.930+2422A=
NM_001166451.1:c.822+2422A=	NP_001159923.1:n.822+2422A=
NM_000893.4:c.930+2422A=	NP_000884.1:n.930+2422A=
NM_001102416.3:c.930+2422A= MANE Select	NP_001095886.1:n.930+2422A=
NM_001166451.2:c.822+2422A=	NP_001159923.1:n.822+2422A=