Canonical Allele Identifier: CA2800665283

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149381_113149383del , CM000675.2:g.113149381_113149383del	GRCh38
NC_000013.10:g.113803695_113803697del , CM000675.1:g.113803695_113803697del	GRCh37
NC_000013.9:g.112851696_112851698del	NCBI36
NG_009258.1:g.31583_31585del , LRG_548:g.31583_31585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1331_1333del MANE Select	ENSP00000364709.3:p.Ala444_Arg445delinsGly
ENST00000375551.7:c.*322_*324del	ENSP00000364701.3:n.*322_*324del
ENST00000375559.7:c.1331_1333del	ENSP00000364709.3:p.Ala444_Arg445delinsGly
ENST00000409306.5:c.*322_*324del	ENSP00000387092.1:n.*322_*324del
NM_000504.3:c.1331_1333del , LRG_548t1:c.1331_1333del	NP_000495.1:p.Ala444_Arg445delinsGly
NM_001312674.1:c.1199_1201del	NP_001299603.1:p.Ala400_Arg401delinsGly
NM_001312675.1:c.*322_*324del	NP_001299604.1:n.*322_*324del
NM_000504.4:c.1331_1333del MANE Select	NP_000495.1:p.Ala444_Arg445delinsGly
NM_001312674.2:c.1199_1201del	NP_001299603.1:p.Ala400_Arg401delinsGly
NM_001312675.2:c.*322_*324del	NP_001299604.1:n.*322_*324del