Canonical Allele Identifier: CA2800665279

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149377_113149378insTTT , CM000675.2:g.113149377_113149378insTTT	GRCh38
NC_000013.10:g.113803691_113803692insTTT , CM000675.1:g.113803691_113803692insTTT	GRCh37
NC_000013.9:g.112851692_112851693insTTT	NCBI36
NG_009258.1:g.31579_31580insTTT , LRG_548:g.31579_31580insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1327_1328insTTT MANE Select	ENSP00000364709.3:p.Gly442_Cys443insPhe
ENST00000375551.7:c.*318_*319insTTT	ENSP00000364701.3:n.*318_*319insTTT
ENST00000375559.7:c.1327_1328insTTT	ENSP00000364709.3:p.Gly442_Cys443insPhe
ENST00000409306.5:c.*318_*319insTTT	ENSP00000387092.1:n.*318_*319insTTT
NM_000504.3:c.1327_1328insTTT , LRG_548t1:c.1327_1328insTTT	NP_000495.1:p.Gly442_Cys443insPhe
NM_001312674.1:c.1195_1196insTTT	NP_001299603.1:p.Gly398_Cys399insPhe
NM_001312675.1:c.*318_*319insTTT	NP_001299604.1:n.*318_*319insTTT
NM_000504.4:c.1327_1328insTTT MANE Select	NP_000495.1:p.Gly442_Cys443insPhe
NM_001312674.2:c.1195_1196insTTT	NP_001299603.1:p.Gly398_Cys399insPhe
NM_001312675.2:c.*318_*319insTTT	NP_001299604.1:n.*318_*319insTTT