Canonical Allele Identifier: CA388793397
Gene: F10 HGNC NCBI

Linked Data

dbSNP Id: rs1332756739

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149208C>G , CM000675.2:g.113149208C>G GRCh38
NC_000013.10:g.113803522C>G , CM000675.1:g.113803522C>G GRCh37
NC_000013.9:g.112851523C>G NCBI36
NG_009258.1:g.31410C>G , LRG_548:g.31410C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1158C>G MANE Select ENSP00000364709.3:p.Asp386Glu
ENST00000375551.7:c.*149C>G ENSP00000364701.3:n.*149C>G
ENST00000375559.7:c.1158C>G ENSP00000364709.3:p.Asp386Glu
ENST00000409306.5:c.*149C>G ENSP00000387092.1:n.*149C>G
NM_000504.3:c.1158C>G , LRG_548t1:c.1158C>G NP_000495.1:p.Asp386Glu
NM_001312674.1:c.1026C>G NP_001299603.1:p.Asp342Glu
NM_001312675.1:c.*149C>G NP_001299604.1:n.*149C>G
NM_000504.4:c.1158C>G MANE Select NP_000495.1:p.Asp386Glu
NM_001312674.2:c.1026C>G NP_001299603.1:p.Asp342Glu
NM_001312675.2:c.*149C>G NP_001299604.1:n.*149C>G