Canonical Allele Identifier: CA2623810294

Gene: F10

Linked Data

• gnomAD v4: 13-113149387-A-ATGATAC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149387_113149388insTGATAC , CM000675.2:g.113149387_113149388insTGATAC	GRCh38
NC_000013.10:g.113803701_113803702insTGATAC , CM000675.1:g.113803701_113803702insTGATAC	GRCh37
NC_000013.9:g.112851702_112851703insTGATAC	NCBI36
NG_009258.1:g.31589_31590insTGATAC , LRG_548:g.31589_31590insTGATAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1337_1338insTGATAC MANE Select	ENSP00000364709.3:p.Lys446delinsAsnAspThr
ENST00000375551.7:c.*328_*329insTGATAC	ENSP00000364701.3:n.*328_*329insTGATAC
ENST00000375559.7:c.1337_1338insTGATAC	ENSP00000364709.3:p.Lys446delinsAsnAspThr
ENST00000409306.5:c.*328_*329insTGATAC	ENSP00000387092.1:n.*328_*329insTGATAC
NM_000504.3:c.1337_1338insTGATAC , LRG_548t1:c.1337_1338insTGATAC	NP_000495.1:p.Lys446delinsAsnAspThr
NM_001312674.1:c.1205_1206insTGATAC	NP_001299603.1:p.Lys402delinsAsnAspThr
NM_001312675.1:c.*328_*329insTGATAC	NP_001299604.1:n.*328_*329insTGATAC
NM_000504.4:c.1337_1338insTGATAC MANE Select	NP_000495.1:p.Lys446delinsAsnAspThr
NM_001312674.2:c.1205_1206insTGATAC	NP_001299603.1:p.Lys402delinsAsnAspThr
NM_001312675.2:c.*328_*329insTGATAC	NP_001299604.1:n.*328_*329insTGATAC