Canonical Allele Identifier: CA2800665316

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149429_113149430insACACACCCAACACA , CM000675.2:g.113149429_113149430insACACACCCAACACA	GRCh38
NC_000013.10:g.113803743_113803744insACACACCCAACACA , CM000675.1:g.113803743_113803744insACACACCCAACACA	GRCh37
NC_000013.9:g.112851744_112851745insACACACCCAACACA	NCBI36
NG_009258.1:g.31631_31632insACACACCCAACACA , LRG_548:g.31631_31632insACACACCCAACACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1379_1380insACACACCCAACACA MANE Select	ENSP00000364709.3:p.Trp461HisfsTer11
ENST00000375551.7:c.*370_*371insACACACCCAACACA	ENSP00000364701.3:n.*370_*371insACACACCCAACACA
ENST00000375559.7:c.1379_1380insACACACCCAACACA	ENSP00000364709.3:p.Trp461HisfsTer11
ENST00000409306.5:c.*370_*371insACACACCCAACACA	ENSP00000387092.1:n.*370_*371insACACACCCAACACA
NM_000504.3:c.1379_1380insACACACCCAACACA , LRG_548t1:c.1379_1380insACACACCCAACACA	NP_000495.1:p.Trp461HisfsTer11
NM_001312674.1:c.1247_1248insACACACCCAACACA	NP_001299603.1:p.Trp417HisfsTer11
NM_001312675.1:c.*370_*371insACACACCCAACACA	NP_001299604.1:n.*370_*371insACACACCCAACACA
NM_000504.4:c.1379_1380insACACACCCAACACA MANE Select	NP_000495.1:p.Trp461HisfsTer11
NM_001312674.2:c.1247_1248insACACACCCAACACA	NP_001299603.1:p.Trp417HisfsTer11
NM_001312675.2:c.*370_*371insACACACCCAACACA	NP_001299604.1:n.*370_*371insACACACCCAACACA