Canonical Allele Identifier: CA2120140425

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149295C= , CM000675.2:g.113149295C=	GRCh38
NC_000013.10:g.113803609C= , CM000675.1:g.113803609C=	GRCh37
NC_000013.9:g.112851610C=	NCBI36
NG_009258.1:g.31497C= , LRG_548:g.31497C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1245C= MANE Select	ENSP00000364709.3:p.Cys415=
ENST00000375551.7:c.*236C=	ENSP00000364701.3:n.*236C=
ENST00000375559.7:c.1245C=	ENSP00000364709.3:p.Cys415=
ENST00000409306.5:c.*236C=	ENSP00000387092.1:n.*236C=
NM_000504.3:c.1245C= , LRG_548t1:c.1245C=	NP_000495.1:p.Cys415=
NM_001312674.1:c.1113C=	NP_001299603.1:p.Cys371=
NM_001312675.1:c.*236C=	NP_001299604.1:n.*236C=
NM_000504.4:c.1245C= MANE Select	NP_000495.1:p.Cys415=
NM_001312674.2:c.1113C=	NP_001299603.1:p.Cys371=
NM_001312675.2:c.*236C=	NP_001299604.1:n.*236C=