Canonical Allele Identifier: CA2800665324

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149252_113149253insACACACCCAACA , CM000675.2:g.113149252_113149253insACACACCCAACA	GRCh38
NC_000013.10:g.113803566_113803567insACACACCCAACA , CM000675.1:g.113803566_113803567insACACACCCAACA	GRCh37
NC_000013.9:g.112851567_112851568insACACACCCAACA	NCBI36
NG_009258.1:g.31454_31455insACACACCCAACA , LRG_548:g.31454_31455insACACACCCAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1202_1203insACACACCCAACA MANE Select	ENSP00000364709.3:p.Asn401delinsLysHisThrGlnHis
ENST00000375551.7:c.*193_*194insACACACCCAACA	ENSP00000364701.3:n.*193_*194insACACACCCAACA
ENST00000375559.7:c.1202_1203insACACACCCAACA	ENSP00000364709.3:p.Asn401delinsLysHisThrGlnHis
ENST00000409306.5:c.*193_*194insACACACCCAACA	ENSP00000387092.1:n.*193_*194insACACACCCAACA
NM_000504.3:c.1202_1203insACACACCCAACA , LRG_548t1:c.1202_1203insACACACCCAACA	NP_000495.1:p.Asn401delinsLysHisThrGlnHis
NM_001312674.1:c.1070_1071insACACACCCAACA	NP_001299603.1:p.Asn357delinsLysHisThrGlnHis
NM_001312675.1:c.*193_*194insACACACCCAACA	NP_001299604.1:n.*193_*194insACACACCCAACA
NM_000504.4:c.1202_1203insACACACCCAACA MANE Select	NP_000495.1:p.Asn401delinsLysHisThrGlnHis
NM_001312674.2:c.1070_1071insACACACCCAACA	NP_001299603.1:p.Asn357delinsLysHisThrGlnHis
NM_001312675.2:c.*193_*194insACACACCCAACA	NP_001299604.1:n.*193_*194insACACACCCAACA