Canonical Allele Identifier: CA2120140669

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149396A= , CM000675.2:g.113149396A=	GRCh38
NC_000013.10:g.113803710A= , CM000675.1:g.113803710A=	GRCh37
NC_000013.9:g.112851711A=	NCBI36
NG_009258.1:g.31598A= , LRG_548:g.31598A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1346A= MANE Select	ENSP00000364709.3:p.Tyr449=
ENST00000375551.7:c.*337A=	ENSP00000364701.3:n.*337A=
ENST00000375559.7:c.1346A=	ENSP00000364709.3:p.Tyr449=
ENST00000409306.5:c.*337A=	ENSP00000387092.1:n.*337A=
NM_000504.3:c.1346A= , LRG_548t1:c.1346A=	NP_000495.1:p.Tyr449=
NM_001312674.1:c.1214A=	NP_001299603.1:p.Tyr405=
NM_001312675.1:c.*337A=	NP_001299604.1:n.*337A=
NM_000504.4:c.1346A= MANE Select	NP_000495.1:p.Tyr449=
NM_001312674.2:c.1214A=	NP_001299603.1:p.Tyr405=
NM_001312675.2:c.*337A=	NP_001299604.1:n.*337A=