Canonical Allele Identifier: CA2120140639

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149385_113149390delinsTAAGGG , CM000675.2:g.113149385_113149390delinsTAAGGG	GRCh38
NC_000013.10:g.113803699_113803704delinsTAAGGG , CM000675.1:g.113803699_113803704delinsTAAGGG	GRCh37
NC_000013.9:g.112851700_112851705delinsTAAGGG	NCBI36
NG_009258.1:g.31587_31592delinsTAAGGG , LRG_548:g.31587_31592delinsTAAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1335_1340delinsTAAGGG MANE Select	ENSP00000364709.3:p.Arg445=
ENST00000375551.7:c.*326_*331delinsTAAGGG	ENSP00000364701.3:n.*326_*331delinsTAAGGG
ENST00000375559.7:c.1335_1340delinsTAAGGG	ENSP00000364709.3:p.Arg445=
ENST00000409306.5:c.*326_*331delinsTAAGGG	ENSP00000387092.1:n.*326_*331delinsTAAGGG
NM_000504.3:c.1335_1340delinsTAAGGG , LRG_548t1:c.1335_1340delinsTAAGGG	NP_000495.1:p.Arg445=
NM_001312674.1:c.1203_1208delinsTAAGGG	NP_001299603.1:p.Arg401=
NM_001312675.1:c.*326_*331delinsTAAGGG	NP_001299604.1:n.*326_*331delinsTAAGGG
NM_000504.4:c.1335_1340delinsTAAGGG MANE Select	NP_000495.1:p.Arg445=
NM_001312674.2:c.1203_1208delinsTAAGGG	NP_001299603.1:p.Arg401=
NM_001312675.2:c.*326_*331delinsTAAGGG	NP_001299604.1:n.*326_*331delinsTAAGGG