Canonical Allele Identifier: CA2120140661

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149392_113149394delinsAAG , CM000675.2:g.113149392_113149394delinsAAG	GRCh38
NC_000013.10:g.113803706_113803708delinsAAG , CM000675.1:g.113803706_113803708delinsAAG	GRCh37
NC_000013.9:g.112851707_112851709delinsAAG	NCBI36
NG_009258.1:g.31594_31596delinsAAG , LRG_548:g.31594_31596delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1342_1344delinsAAG MANE Select	ENSP00000364709.3:p.Lys448=
ENST00000375551.7:c.*333_*335delinsAAG	ENSP00000364701.3:n.*333_*335delinsAAG
ENST00000375559.7:c.1342_1344delinsAAG	ENSP00000364709.3:p.Lys448=
ENST00000409306.5:c.*333_*335delinsAAG	ENSP00000387092.1:n.*333_*335delinsAAG
NM_000504.3:c.1342_1344delinsAAG , LRG_548t1:c.1342_1344delinsAAG	NP_000495.1:p.Lys448=
NM_001312674.1:c.1210_1212delinsAAG	NP_001299603.1:p.Lys404=
NM_001312675.1:c.*333_*335delinsAAG	NP_001299604.1:n.*333_*335delinsAAG
NM_000504.4:c.1342_1344delinsAAG MANE Select	NP_000495.1:p.Lys448=
NM_001312674.2:c.1210_1212delinsAAG	NP_001299603.1:p.Lys404=
NM_001312675.2:c.*333_*335delinsAAG	NP_001299604.1:n.*333_*335delinsAAG