Canonical Allele Identifier: CA2623810275

Gene: F10

Linked Data

• gnomAD v4: 13-113149384-G-GTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149385_113149386insTTTTT , CM000675.2:g.113149385_113149386insTTTTT	GRCh38
NC_000013.10:g.113803699_113803700insTTTTT , CM000675.1:g.113803699_113803700insTTTTT	GRCh37
NC_000013.9:g.112851700_112851701insTTTTT	NCBI36
NG_009258.1:g.31587_31588insTTTTT , LRG_548:g.31587_31588insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1335_1336insTTTTT MANE Select	ENSP00000364709.3:p.Lys446PhefsTer23
ENST00000375551.7:c.*326_*327insTTTTT	ENSP00000364701.3:n.*326_*327insTTTTT
ENST00000375559.7:c.1335_1336insTTTTT	ENSP00000364709.3:p.Lys446PhefsTer23
ENST00000409306.5:c.*326_*327insTTTTT	ENSP00000387092.1:n.*326_*327insTTTTT
NM_000504.3:c.1335_1336insTTTTT , LRG_548t1:c.1335_1336insTTTTT	NP_000495.1:p.Lys446PhefsTer23
NM_001312674.1:c.1203_1204insTTTTT	NP_001299603.1:p.Lys402PhefsTer23
NM_001312675.1:c.*326_*327insTTTTT	NP_001299604.1:n.*326_*327insTTTTT
NM_000504.4:c.1335_1336insTTTTT MANE Select	NP_000495.1:p.Lys446PhefsTer23
NM_001312674.2:c.1203_1204insTTTTT	NP_001299603.1:p.Lys402PhefsTer23
NM_001312675.2:c.*326_*327insTTTTT	NP_001299604.1:n.*326_*327insTTTTT