Canonical Allele Identifier: CA2120140061

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149056A= , CM000675.2:g.113149056A=	GRCh38
NC_000013.10:g.113803370A= , CM000675.1:g.113803370A=	GRCh37
NC_000013.9:g.112851371A=	NCBI36
NG_009258.1:g.31258A= , LRG_548:g.31258A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.1006A= MANE Select	ENSP00000364709.3:p.Met336=
ENST00000375551.7:c.996A=	ENSP00000364701.3:p.Ala332=
ENST00000375559.7:c.1006A=	ENSP00000364709.3:p.Met336=
ENST00000409306.5:c.1002A=	ENSP00000387092.1:p.Ala334=
NM_000504.3:c.1006A= , LRG_548t1:c.1006A=	NP_000495.1:p.Met336=
NM_001312674.1:c.874A=	NP_001299603.1:p.Met292=
NM_001312675.1:c.996A=	NP_001299604.1:p.Ala332=
NM_000504.4:c.1006A= MANE Select	NP_000495.1:p.Met336=
NM_001312674.2:c.874A=	NP_001299603.1:p.Met292=
NM_001312675.2:c.996A=	NP_001299604.1:p.Ala332=