Canonical Allele Identifier: CA2623810233
Gene: F10 HGNC NCBI

Linked Data

gnomAD v4: 13-113149377-TGTGCCC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149380_113149385del , CM000675.2:g.113149380_113149385del GRCh38
NC_000013.10:g.113803694_113803699del , CM000675.1:g.113803694_113803699del GRCh37
NC_000013.9:g.112851695_112851700del NCBI36
NG_009258.1:g.31582_31587del , LRG_548:g.31582_31587del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1330_1335del MANE Select ENSP00000364709.3:p.Ala444_Arg445del
ENST00000375551.7:c.*321_*326del ENSP00000364701.3:n.*321_*326del
ENST00000375559.7:c.1330_1335del ENSP00000364709.3:p.Ala444_Arg445del
ENST00000409306.5:c.*321_*326del ENSP00000387092.1:n.*321_*326del
NM_000504.3:c.1330_1335del , LRG_548t1:c.1330_1335del NP_000495.1:p.Ala444_Arg445del
NM_001312674.1:c.1198_1203del NP_001299603.1:p.Ala400_Arg401del
NM_001312675.1:c.*321_*326del NP_001299604.1:n.*321_*326del
NM_000504.4:c.1330_1335del MANE Select NP_000495.1:p.Ala444_Arg445del
NM_001312674.2:c.1198_1203del NP_001299603.1:p.Ala400_Arg401del
NM_001312675.2:c.*321_*326del NP_001299604.1:n.*321_*326del
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