Canonical Allele Identifier: CA612868389

Gene: F10

Linked Data

• gnomAD v2: 13-113803698-G-GTTTTTTTTT
• MyVariant Identifiers: chr13:g.113803698_113803699insTTTTTTTTT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149385_113149386insTTTTTTTTT , CM000675.2:g.113149385_113149386insTTTTTTTTT	GRCh38
NC_000013.10:g.113803699_113803700insTTTTTTTTT , CM000675.1:g.113803699_113803700insTTTTTTTTT	GRCh37
NC_000013.9:g.112851700_112851701insTTTTTTTTT	NCBI36
NG_009258.1:g.31587_31588insTTTTTTTTT , LRG_548:g.31587_31588insTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1335_1336insTTTTTTTTT MANE Select	ENSP00000364709.3:p.Arg445_Lys446insPhePhePhe
ENST00000375551.7:c.*326_*327insTTTTTTTTT	ENSP00000364701.3:n.*326_*327insTTTTTTTTT
ENST00000375559.7:c.1335_1336insTTTTTTTTT	ENSP00000364709.3:p.Arg445_Lys446insPhePhePhe
ENST00000409306.5:c.*326_*327insTTTTTTTTT	ENSP00000387092.1:n.*326_*327insTTTTTTTTT
NM_000504.3:c.1335_1336insTTTTTTTTT , LRG_548t1:c.1335_1336insTTTTTTTTT	NP_000495.1:p.Arg445_Lys446insPhePhePhe
NM_001312674.1:c.1203_1204insTTTTTTTTT	NP_001299603.1:p.Arg401_Lys402insPhePhePhe
NM_001312675.1:c.*326_*327insTTTTTTTTT	NP_001299604.1:n.*326_*327insTTTTTTTTT
NM_000504.4:c.1335_1336insTTTTTTTTT MANE Select	NP_000495.1:p.Arg445_Lys446insPhePhePhe
NM_001312674.2:c.1203_1204insTTTTTTTTT	NP_001299603.1:p.Arg401_Lys402insPhePhePhe
NM_001312675.2:c.*326_*327insTTTTTTTTT	NP_001299604.1:n.*326_*327insTTTTTTTTT