Canonical Allele Identifier: CA612868382

Gene: F10

Linked Data

• gnomAD v2: 13-113803693-TGCCCGTAAGGG-T
• gnomAD v3: 13-113149379-TGCCCGTAAGGG-T
• gnomAD v4: 13-113149379-TGCCCGTAAGGG-T
• MyVariant Identifiers: chr13:g.113803694_113803704del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149381_113149391del , CM000675.2:g.113149381_113149391del	GRCh38
NC_000013.10:g.113803695_113803705del , CM000675.1:g.113803695_113803705del	GRCh37
NC_000013.9:g.112851696_112851706del	NCBI36
NG_009258.1:g.31583_31593del , LRG_548:g.31583_31593del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1331_1341del MANE Select	ENSP00000364709.3:p.Ala444GlufsTer?
ENST00000375551.7:c.*322_*332del	ENSP00000364701.3:n.*322_*332del
ENST00000375559.7:c.1331_1341del	ENSP00000364709.3:p.Ala444GlufsTer?
ENST00000409306.5:c.*322_*332del	ENSP00000387092.1:n.*322_*332del
NM_000504.3:c.1331_1341del , LRG_548t1:c.1331_1341del	NP_000495.1:p.Ala444GlufsTer?
NM_001312674.1:c.1199_1209del	NP_001299603.1:p.Ala400GlufsTer?
NM_001312675.1:c.*322_*332del	NP_001299604.1:n.*322_*332del
NM_000504.4:c.1331_1341del MANE Select	NP_000495.1:p.Ala444GlufsTer?
NM_001312674.2:c.1199_1209del	NP_001299603.1:p.Ala400GlufsTer?
NM_001312675.2:c.*322_*332del	NP_001299604.1:n.*322_*332del