Canonical Allele Identifier: CA612868390

Gene: F10

Linked Data

• dbSNP Id: rs1196291054
• gnomAD v2: 13-113803699-TAAGGG-T
• gnomAD v3: 13-113149385-TAAGGG-T
• gnomAD v4: 13-113149385-TAAGGG-T
• MyVariant Identifiers: chr13:g.113803700_113803704del (hg19) ; chr13:g.113149386_113149390del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149386_113149390del , CM000675.2:g.113149386_113149390del	GRCh38
NC_000013.10:g.113803700_113803704del , CM000675.1:g.113803700_113803704del	GRCh37
NC_000013.9:g.112851701_112851705del	NCBI36
NG_009258.1:g.31588_31592del , LRG_548:g.31588_31592del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1336_1340del MANE Select	ENSP00000364709.3:p.Lys446GlufsTer?
ENST00000375551.7:c.*327_*331del	ENSP00000364701.3:n.*327_*331del
ENST00000375559.7:c.1336_1340del	ENSP00000364709.3:p.Lys446GlufsTer?
ENST00000409306.5:c.*327_*331del	ENSP00000387092.1:n.*327_*331del
NM_000504.3:c.1336_1340del , LRG_548t1:c.1336_1340del	NP_000495.1:p.Lys446GlufsTer?
NM_001312674.1:c.1204_1208del	NP_001299603.1:p.Lys402GlufsTer?
NM_001312675.1:c.*327_*331del	NP_001299604.1:n.*327_*331del
NM_000504.4:c.1336_1340del MANE Select	NP_000495.1:p.Lys446GlufsTer?
NM_001312674.2:c.1204_1208del	NP_001299603.1:p.Lys402GlufsTer?
NM_001312675.2:c.*327_*331del	NP_001299604.1:n.*327_*331del