Canonical Allele Identifier: CA915940388

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149272_113149274del , CM000675.2:g.113149272_113149274del	GRCh38
NC_000013.10:g.113803586_113803588del , CM000675.1:g.113803586_113803588del	GRCh37
NC_000013.9:g.112851587_112851589del	NCBI36
NG_009258.1:g.31474_31476del , LRG_548:g.31474_31476del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1222_1224del MANE Select	ENSP00000364709.3:p.Asp408del
ENST00000375551.7:c.*213_*215del	ENSP00000364701.3:n.*213_*215del
ENST00000375559.7:c.1222_1224del	ENSP00000364709.3:p.Asp408del
ENST00000409306.5:c.*213_*215del	ENSP00000387092.1:n.*213_*215del
NM_000504.3:c.1222_1224del , LRG_548t1:c.1222_1224del	NP_000495.1:p.Asp408del
NM_001312674.1:c.1090_1092del	NP_001299603.1:p.Asp364del
NM_001312675.1:c.*213_*215del	NP_001299604.1:n.*213_*215del
NM_000504.4:c.1222_1224del MANE Select	NP_000495.1:p.Asp408del
NM_001312674.2:c.1090_1092del	NP_001299603.1:p.Asp364del
NM_001312675.2:c.*213_*215del	NP_001299604.1:n.*213_*215del