Canonical Allele Identifier: CA2830665552

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149342_113149345del , CM000675.2:g.113149342_113149345del	GRCh38
NC_000013.10:g.113803656_113803659del , CM000675.1:g.113803656_113803659del	GRCh37
NC_000013.9:g.112851657_112851660del	NCBI36
NG_009258.1:g.31544_31547del , LRG_548:g.31544_31547del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1292_1295del MANE Select	ENSP00000364709.3:p.Tyr431SerfsTer2
ENST00000375551.7:c.*283_*286del	ENSP00000364701.3:n.*283_*286del
ENST00000375559.7:c.1292_1295del	ENSP00000364709.3:p.Tyr431SerfsTer2
ENST00000409306.5:c.*283_*286del	ENSP00000387092.1:n.*283_*286del
NM_000504.3:c.1292_1295del , LRG_548t1:c.1292_1295del	NP_000495.1:p.Tyr431SerfsTer2
NM_001312674.1:c.1160_1163del	NP_001299603.1:p.Tyr387SerfsTer2
NM_001312675.1:c.*283_*286del	NP_001299604.1:n.*283_*286del
NM_000504.4:c.1292_1295del MANE Select	NP_000495.1:p.Tyr431SerfsTer2
NM_001312674.2:c.1160_1163del	NP_001299603.1:p.Tyr387SerfsTer2
NM_001312675.2:c.*283_*286del	NP_001299604.1:n.*283_*286del