Canonical Allele Identifier: CA2800665256

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149368_113149376del , CM000675.2:g.113149368_113149376del	GRCh38
NC_000013.10:g.113803682_113803690del , CM000675.1:g.113803682_113803690del	GRCh37
NC_000013.9:g.112851683_112851691del	NCBI36
NG_009258.1:g.31570_31578del , LRG_548:g.31570_31578del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1318_1326del MANE Select	ENSP00000364709.3:p.Gly440_Gly442del
ENST00000375551.7:c.*309_*317del	ENSP00000364701.3:n.*309_*317del
ENST00000375559.7:c.1318_1326del	ENSP00000364709.3:p.Gly440_Gly442del
ENST00000409306.5:c.*309_*317del	ENSP00000387092.1:n.*309_*317del
NM_000504.3:c.1318_1326del , LRG_548t1:c.1318_1326del	NP_000495.1:p.Gly440_Gly442del
NM_001312674.1:c.1186_1194del	NP_001299603.1:p.Gly396_Gly398del
NM_001312675.1:c.*309_*317del	NP_001299604.1:n.*309_*317del
NM_000504.4:c.1318_1326del MANE Select	NP_000495.1:p.Gly440_Gly442del
NM_001312674.2:c.1186_1194del	NP_001299603.1:p.Gly396_Gly398del
NM_001312675.2:c.*309_*317del	NP_001299604.1:n.*309_*317del