Canonical Allele Identifier: CA2800665289

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149384_113149385insATGA , CM000675.2:g.113149384_113149385insATGA	GRCh38
NC_000013.10:g.113803698_113803699insATGA , CM000675.1:g.113803698_113803699insATGA	GRCh37
NC_000013.9:g.112851699_112851700insATGA	NCBI36
NG_009258.1:g.31586_31587insATGA , LRG_548:g.31586_31587insATGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1334_1335insATGA MANE Select	ENSP00000364709.3:p.Lys446Ter
ENST00000375551.7:c.*325_*326insATGA	ENSP00000364701.3:n.*325_*326insATGA
ENST00000375559.7:c.1334_1335insATGA	ENSP00000364709.3:p.Lys446Ter
ENST00000409306.5:c.*325_*326insATGA	ENSP00000387092.1:n.*325_*326insATGA
NM_000504.3:c.1334_1335insATGA , LRG_548t1:c.1334_1335insATGA	NP_000495.1:p.Lys446Ter
NM_001312674.1:c.1202_1203insATGA	NP_001299603.1:p.Lys402Ter
NM_001312675.1:c.*325_*326insATGA	NP_001299604.1:n.*325_*326insATGA
NM_000504.4:c.1334_1335insATGA MANE Select	NP_000495.1:p.Lys446Ter
NM_001312674.2:c.1202_1203insATGA	NP_001299603.1:p.Lys402Ter
NM_001312675.2:c.*325_*326insATGA	NP_001299604.1:n.*325_*326insATGA