Canonical Allele Identifier: CA2120140078

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149062G= , CM000675.2:g.113149062G=	GRCh38
NC_000013.10:g.113803376G= , CM000675.1:g.113803376G=	GRCh37
NC_000013.9:g.112851377G=	NCBI36
NG_009258.1:g.31264G= , LRG_548:g.31264G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.1012G= MANE Select	ENSP00000364709.3:p.Val338=
ENST00000375551.7:c.*3G=	ENSP00000364701.3:n.*3G=
ENST00000375559.7:c.1012G=	ENSP00000364709.3:p.Val338=
ENST00000409306.5:c.*3G=	ENSP00000387092.1:n.*3G=
NM_000504.3:c.1012G= , LRG_548t1:c.1012G=	NP_000495.1:p.Val338=
NM_001312674.1:c.880G=	NP_001299603.1:p.Val294=
NM_001312675.1:c.*3G=	NP_001299604.1:n.*3G=
NM_000504.4:c.1012G= MANE Select	NP_000495.1:p.Val338=
NM_001312674.2:c.880G=	NP_001299603.1:p.Val294=
NM_001312675.2:c.*3G=	NP_001299604.1:n.*3G=