Canonical Allele Identifier: CA612868391

Gene: F10

Linked Data

• dbSNP Id: rs1314809840
• gnomAD v2: 13-113803701-AGG-A
• gnomAD v3: 13-113149387-AGG-A
• gnomAD v4: 13-113149387-AGG-A
• MyVariant Identifiers: chr13:g.113803702_113803703del (hg19) ; chr13:g.113149388_113149389del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149390_113149391del , CM000675.2:g.113149390_113149391del	GRCh38
NC_000013.10:g.113803704_113803705del , CM000675.1:g.113803704_113803705del	GRCh37
NC_000013.9:g.112851705_112851706del	NCBI36
NG_009258.1:g.31592_31593del , LRG_548:g.31592_31593del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1340_1341del MANE Select	ENSP00000364709.3:p.Gly447GlufsTer?
ENST00000375551.7:c.*331_*332del	ENSP00000364701.3:n.*331_*332del
ENST00000375559.7:c.1340_1341del	ENSP00000364709.3:p.Gly447GlufsTer?
ENST00000409306.5:c.*331_*332del	ENSP00000387092.1:n.*331_*332del
NM_000504.3:c.1340_1341del , LRG_548t1:c.1340_1341del	NP_000495.1:p.Gly447GlufsTer?
NM_001312674.1:c.1208_1209del	NP_001299603.1:p.Gly403GlufsTer?
NM_001312675.1:c.*331_*332del	NP_001299604.1:n.*331_*332del
NM_000504.4:c.1340_1341del MANE Select	NP_000495.1:p.Gly447GlufsTer?
NM_001312674.2:c.1208_1209del	NP_001299603.1:p.Gly403GlufsTer?
NM_001312675.2:c.*331_*332del	NP_001299604.1:n.*331_*332del