Canonical Allele Identifier: CA2800665298

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149387_113149388insTCATAC , CM000675.2:g.113149387_113149388insTCATAC	GRCh38
NC_000013.10:g.113803701_113803702insTCATAC , CM000675.1:g.113803701_113803702insTCATAC	GRCh37
NC_000013.9:g.112851702_112851703insTCATAC	NCBI36
NG_009258.1:g.31589_31590insTCATAC , LRG_548:g.31589_31590insTCATAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1337_1338insTCATAC MANE Select	ENSP00000364709.3:p.Lys446delinsAsnHisThr
ENST00000375551.7:c.*328_*329insTCATAC	ENSP00000364701.3:n.*328_*329insTCATAC
ENST00000375559.7:c.1337_1338insTCATAC	ENSP00000364709.3:p.Lys446delinsAsnHisThr
ENST00000409306.5:c.*328_*329insTCATAC	ENSP00000387092.1:n.*328_*329insTCATAC
NM_000504.3:c.1337_1338insTCATAC , LRG_548t1:c.1337_1338insTCATAC	NP_000495.1:p.Lys446delinsAsnHisThr
NM_001312674.1:c.1205_1206insTCATAC	NP_001299603.1:p.Lys402delinsAsnHisThr
NM_001312675.1:c.*328_*329insTCATAC	NP_001299604.1:n.*328_*329insTCATAC
NM_000504.4:c.1337_1338insTCATAC MANE Select	NP_000495.1:p.Lys446delinsAsnHisThr
NM_001312674.2:c.1205_1206insTCATAC	NP_001299603.1:p.Lys402delinsAsnHisThr
NM_001312675.2:c.*328_*329insTCATAC	NP_001299604.1:n.*328_*329insTCATAC