Canonical Allele Identifier: CA612868387

Gene: F10

Linked Data

• dbSNP Id: rs1306002356
• gnomAD v2: 13-113803698-G-GTT
• gnomAD v3: 13-113149384-G-GTT
• gnomAD v4: 13-113149384-G-GTT
• MyVariant Identifiers: chr13:g.113803698_113803699insTT (hg19) ; chr13:g.113149384_113149385insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149385_113149386insTT , CM000675.2:g.113149385_113149386insTT	GRCh38
NC_000013.10:g.113803699_113803700insTT , CM000675.1:g.113803699_113803700insTT	GRCh37
NC_000013.9:g.112851700_112851701insTT	NCBI36
NG_009258.1:g.31587_31588insTT , LRG_548:g.31587_31588insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1335_1336insTT MANE Select	ENSP00000364709.3:p.Lys446LeufsTer22
ENST00000375551.7:c.*326_*327insTT	ENSP00000364701.3:n.*326_*327insTT
ENST00000375559.7:c.1335_1336insTT	ENSP00000364709.3:p.Lys446LeufsTer22
ENST00000409306.5:c.*326_*327insTT	ENSP00000387092.1:n.*326_*327insTT
NM_000504.3:c.1335_1336insTT , LRG_548t1:c.1335_1336insTT	NP_000495.1:p.Lys446LeufsTer22
NM_001312674.1:c.1203_1204insTT	NP_001299603.1:p.Lys402LeufsTer22
NM_001312675.1:c.*326_*327insTT	NP_001299604.1:n.*326_*327insTT
NM_000504.4:c.1335_1336insTT MANE Select	NP_000495.1:p.Lys446LeufsTer22
NM_001312674.2:c.1203_1204insTT	NP_001299603.1:p.Lys402LeufsTer22
NM_001312675.2:c.*326_*327insTT	NP_001299604.1:n.*326_*327insTT