Canonical Allele Identifier: CA388794411
Gene: F10 HGNC NCBI

Linked Data

dbSNP Id: rs1566922905

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149414T>C , CM000675.2:g.113149414T>C GRCh38
NC_000013.10:g.113803728T>C , CM000675.1:g.113803728T>C GRCh37
NC_000013.9:g.112851729T>C NCBI36
NG_009258.1:g.31616T>C , LRG_548:g.31616T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1364T>C MANE Select ENSP00000364709.3:p.Val455Ala
ENST00000375551.7:c.*355T>C ENSP00000364701.3:n.*355T>C
ENST00000375559.7:c.1364T>C ENSP00000364709.3:p.Val455Ala
ENST00000409306.5:c.*355T>C ENSP00000387092.1:n.*355T>C
NM_000504.3:c.1364T>C , LRG_548t1:c.1364T>C NP_000495.1:p.Val455Ala
NM_001312674.1:c.1232T>C NP_001299603.1:p.Val411Ala
NM_001312675.1:c.*355T>C NP_001299604.1:n.*355T>C
NM_000504.4:c.1364T>C MANE Select NP_000495.1:p.Val455Ala
NM_001312674.2:c.1232T>C NP_001299603.1:p.Val411Ala
NM_001312675.2:c.*355T>C NP_001299604.1:n.*355T>C