Canonical Allele Identifier: CA1969072191

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726032C= , CM000673.2:g.46726032C=	GRCh38
NC_000011.9:g.46747582C= , CM000673.1:g.46747582C=	GRCh37
NC_000011.8:g.46704158C=	NCBI36
NG_008953.1:g.11840C= , LRG_551:g.11840C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.733C= MANE Select	ENSP00000308541.5:p.Leu245=
ENST00000311907.9:c.733C=	ENSP00000308541.5:p.Leu245=
ENST00000442468.1:c.703C=	ENSP00000387413.1:p.Leu235=
ENST00000490274.1:n.513C=
ENST00000530231.5:c.733C=	ENSP00000433907.1:p.Leu245=
NM_000506.3:c.733C=	NP_000497.1:p.Leu245=
NM_000506.4:c.733C= , LRG_551t1:c.733C=	NP_000497.1:p.Leu245=
NM_001311257.1:c.685C=	NP_001298186.1:p.Leu229=
XR_428840.2:n.777C=
XR_428840.4:n.768C=
NM_000506.5:c.733C= MANE Select	NP_000497.1:p.Leu245=
NM_001311257.2:c.685C=	NP_001298186.1:p.Leu229=