Canonical Allele Identifier: CA2623810242

Gene: F10

Linked Data

• gnomAD v4: 13-113149379-TGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149380_113149382del , CM000675.2:g.113149380_113149382del	GRCh38
NC_000013.10:g.113803694_113803696del , CM000675.1:g.113803694_113803696del	GRCh37
NC_000013.9:g.112851695_112851697del	NCBI36
NG_009258.1:g.31582_31584del , LRG_548:g.31582_31584del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1330_1332del MANE Select	ENSP00000364709.3:p.Ala444del
ENST00000375551.7:c.*321_*323del	ENSP00000364701.3:n.*321_*323del
ENST00000375559.7:c.1330_1332del	ENSP00000364709.3:p.Ala444del
ENST00000409306.5:c.*321_*323del	ENSP00000387092.1:n.*321_*323del
NM_000504.3:c.1330_1332del , LRG_548t1:c.1330_1332del	NP_000495.1:p.Ala444del
NM_001312674.1:c.1198_1200del	NP_001299603.1:p.Ala400del
NM_001312675.1:c.*321_*323del	NP_001299604.1:n.*321_*323del
NM_000504.4:c.1330_1332del MANE Select	NP_000495.1:p.Ala444del
NM_001312674.2:c.1198_1200del	NP_001299603.1:p.Ala400del
NM_001312675.2:c.*321_*323del	NP_001299604.1:n.*321_*323del