Canonical Allele Identifier: CA2120140609

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149379_113149384delinsTGCCCG , CM000675.2:g.113149379_113149384delinsTGCCCG	GRCh38
NC_000013.10:g.113803693_113803698delinsTGCCCG , CM000675.1:g.113803693_113803698delinsTGCCCG	GRCh37
NC_000013.9:g.112851694_112851699delinsTGCCCG	NCBI36
NG_009258.1:g.31581_31586delinsTGCCCG , LRG_548:g.31581_31586delinsTGCCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1329_1334delinsTGCCCG MANE Select	ENSP00000364709.3:p.Cys443=
ENST00000375551.7:c.*320_*325delinsTGCCCG	ENSP00000364701.3:n.*320_*325delinsTGCCCG
ENST00000375559.7:c.1329_1334delinsTGCCCG	ENSP00000364709.3:p.Cys443=
ENST00000409306.5:c.*320_*325delinsTGCCCG	ENSP00000387092.1:n.*320_*325delinsTGCCCG
NM_000504.3:c.1329_1334delinsTGCCCG , LRG_548t1:c.1329_1334delinsTGCCCG	NP_000495.1:p.Cys443=
NM_001312674.1:c.1197_1202delinsTGCCCG	NP_001299603.1:p.Cys399=
NM_001312675.1:c.*320_*325delinsTGCCCG	NP_001299604.1:n.*320_*325delinsTGCCCG
NM_000504.4:c.1329_1334delinsTGCCCG MANE Select	NP_000495.1:p.Cys443=
NM_001312674.2:c.1197_1202delinsTGCCCG	NP_001299603.1:p.Cys399=
NM_001312675.2:c.*320_*325delinsTGCCCG	NP_001299604.1:n.*320_*325delinsTGCCCG