Canonical Allele Identifier: CA2120140329

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149215A= , CM000675.2:g.113149215A=	GRCh38
NC_000013.10:g.113803529A= , CM000675.1:g.113803529A=	GRCh37
NC_000013.9:g.112851530A=	NCBI36
NG_009258.1:g.31417A= , LRG_548:g.31417A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1165A= MANE Select	ENSP00000364709.3:p.Ser389=
ENST00000375551.7:c.*156A=	ENSP00000364701.3:n.*156A=
ENST00000375559.7:c.1165A=	ENSP00000364709.3:p.Ser389=
ENST00000409306.5:c.*156A=	ENSP00000387092.1:n.*156A=
NM_000504.3:c.1165A= , LRG_548t1:c.1165A=	NP_000495.1:p.Ser389=
NM_001312674.1:c.1033A=	NP_001299603.1:p.Ser345=
NM_001312675.1:c.*156A=	NP_001299604.1:n.*156A=
NM_000504.4:c.1165A= MANE Select	NP_000495.1:p.Ser389=
NM_001312674.2:c.1033A=	NP_001299603.1:p.Ser345=
NM_001312675.2:c.*156A=	NP_001299604.1:n.*156A=