Canonical Allele Identifier: CA2623810235

Gene: F10

Linked Data

• gnomAD v4: 13-113149378-GTGCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149379_113149383del , CM000675.2:g.113149379_113149383del	GRCh38
NC_000013.10:g.113803693_113803697del , CM000675.1:g.113803693_113803697del	GRCh37
NC_000013.9:g.112851694_112851698del	NCBI36
NG_009258.1:g.31581_31585del , LRG_548:g.31581_31585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1329_1333del MANE Select	ENSP00000364709.3:p.Cys443TrpfsTer2
ENST00000375551.7:c.*320_*324del	ENSP00000364701.3:n.*320_*324del
ENST00000375559.7:c.1329_1333del	ENSP00000364709.3:p.Cys443TrpfsTer2
ENST00000409306.5:c.*320_*324del	ENSP00000387092.1:n.*320_*324del
NM_000504.3:c.1329_1333del , LRG_548t1:c.1329_1333del	NP_000495.1:p.Cys443TrpfsTer2
NM_001312674.1:c.1197_1201del	NP_001299603.1:p.Cys399TrpfsTer2
NM_001312675.1:c.*320_*324del	NP_001299604.1:n.*320_*324del
NM_000504.4:c.1329_1333del MANE Select	NP_000495.1:p.Cys443TrpfsTer2
NM_001312674.2:c.1197_1201del	NP_001299603.1:p.Cys399TrpfsTer2
NM_001312675.2:c.*320_*324del	NP_001299604.1:n.*320_*324del