Canonical Allele Identifier: CA960419809

Gene: F10

Linked Data

• gnomAD v3: 13-113149377-TG-T
• gnomAD v4: 13-113149377-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149378del , CM000675.2:g.113149378del	GRCh38
NC_000013.10:g.113803692del , CM000675.1:g.113803692del	GRCh37
NC_000013.9:g.112851693del	NCBI36
NG_009258.1:g.31580del , LRG_548:g.31580del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1328del MANE Select	ENSP00000364709.3:p.Cys443LeufsTer24
ENST00000375551.7:c.*319del	ENSP00000364701.3:n.*319del
ENST00000375559.7:c.1328del	ENSP00000364709.3:p.Cys443LeufsTer24
ENST00000409306.5:c.*319del	ENSP00000387092.1:n.*319del
NM_000504.3:c.1328del , LRG_548t1:c.1328del	NP_000495.1:p.Cys443LeufsTer24
NM_001312674.1:c.1196del	NP_001299603.1:p.Cys399LeufsTer24
NM_001312675.1:c.*319del	NP_001299604.1:n.*319del
NM_000504.4:c.1328del MANE Select	NP_000495.1:p.Cys443LeufsTer24
NM_001312674.2:c.1196del	NP_001299603.1:p.Cys399LeufsTer24
NM_001312675.2:c.*319del	NP_001299604.1:n.*319del