Canonical Allele Identifier: CA2832561764

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149312dup , CM000675.2:g.113149312dup	GRCh38
NC_000013.10:g.113803626dup , CM000675.1:g.113803626dup	GRCh37
NC_000013.9:g.112851627dup	NCBI36
NG_009258.1:g.31514dup , LRG_548:g.31514dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1262dup MANE Select	ENSP00000364709.3:p.His423AlafsTer24
ENST00000375551.7:c.*253dup	ENSP00000364701.3:n.*253dup
ENST00000375559.7:c.1262dup	ENSP00000364709.3:p.His423AlafsTer24
ENST00000409306.5:c.*253dup	ENSP00000387092.1:n.*253dup
NM_000504.3:c.1262dup , LRG_548t1:c.1262dup	NP_000495.1:p.His423AlafsTer24
NM_001312674.1:c.1130dup	NP_001299603.1:p.His379AlafsTer24
NM_001312675.1:c.*253dup	NP_001299604.1:n.*253dup
NM_000504.4:c.1262dup MANE Select	NP_000495.1:p.His423AlafsTer24
NM_001312674.2:c.1130dup	NP_001299603.1:p.His379AlafsTer24
NM_001312675.2:c.*253dup	NP_001299604.1:n.*253dup