Canonical Allele Identifier: CA2120128105

Gene: F10

Linked Data

• dbSNP Id: rs1595093482

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113139542T>G , CM000675.2:g.113139542T>G	GRCh38
NC_000013.10:g.113793856T>G , CM000675.1:g.113793856T>G	GRCh37
NC_000013.9:g.112841857T>G	NCBI36
NG_009258.1:g.21744T>G , LRG_548:g.21744T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.370+72T>G MANE Select	ENSP00000364709.3:n.370+72T>G
ENST00000375551.7:c.370+72T>G	ENSP00000364701.3:n.370+72T>G
ENST00000375559.7:c.370+72T>G	ENSP00000364709.3:n.370+72T>G
ENST00000409306.5:c.370+72T>G	ENSP00000387092.1:n.370+72T>G
ENST00000410083.6:c.370+72T>G	ENSP00000386320.2:n.370+72T>G
ENST00000477269.5:n.407+72T>G
NM_000504.3:c.370+72T>G , LRG_548t1:c.370+72T>G	NP_000495.1:n.370+72T>G
NM_001312674.1:c.370+72T>G	NP_001299603.1:n.370+72T>G
NM_001312675.1:c.370+72T>G	NP_001299604.1:n.370+72T>G
NM_000504.4:c.370+72T>G MANE Select	NP_000495.1:n.370+72T>G
NM_001312674.2:c.370+72T>G	NP_001299603.1:n.370+72T>G
NM_001312675.2:c.370+72T>G	NP_001299604.1:n.370+72T>G