Canonical Allele Identifier: CA2120140701

Gene: F10

Linked Data

• dbSNP Id: rs2036619544

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149405_113149418del , CM000675.2:g.113149405_113149418del	GRCh38
NC_000013.10:g.113803719_113803732del , CM000675.1:g.113803719_113803732del	GRCh37
NC_000013.9:g.112851720_112851733del	NCBI36
NG_009258.1:g.31607_31620del , LRG_548:g.31607_31620del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1355_1368del MANE Select	ENSP00000364709.3:p.Tyr452CysfsTer?
ENST00000375551.7:c.*346_*359del	ENSP00000364701.3:n.*346_*359del
ENST00000375559.7:c.1355_1368del	ENSP00000364709.3:p.Tyr452CysfsTer?
ENST00000409306.5:c.*346_*359del	ENSP00000387092.1:n.*346_*359del
NM_000504.3:c.1355_1368del , LRG_548t1:c.1355_1368del	NP_000495.1:p.Tyr452CysfsTer?
NM_001312674.1:c.1223_1236del	NP_001299603.1:p.Tyr408CysfsTer?
NM_001312675.1:c.*346_*359del	NP_001299604.1:n.*346_*359del
NM_000504.4:c.1355_1368del MANE Select	NP_000495.1:p.Tyr452CysfsTer?
NM_001312674.2:c.1223_1236del	NP_001299603.1:p.Tyr408CysfsTer?
NM_001312675.2:c.*346_*359del	NP_001299604.1:n.*346_*359del