Canonical Allele Identifier: CA388794353
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 626926
ClinVar RCV Id: RCV000851588
dbSNP Id: rs1595099844

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149398G>A , CM000675.2:g.113149398G>A GRCh38
NC_000013.10:g.113803712G>A , CM000675.1:g.113803712G>A GRCh37
NC_000013.9:g.112851713G>A NCBI36
NG_009258.1:g.31600G>A , LRG_548:g.31600G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1348G>A MANE Select ENSP00000364709.3:p.Gly450Arg
ENST00000375551.7:c.*339G>A ENSP00000364701.3:n.*339G>A
ENST00000375559.7:c.1348G>A ENSP00000364709.3:p.Gly450Arg
ENST00000409306.5:c.*339G>A ENSP00000387092.1:n.*339G>A
NM_000504.3:c.1348G>A , LRG_548t1:c.1348G>A NP_000495.1:p.Gly450Arg
NM_001312674.1:c.1216G>A NP_001299603.1:p.Gly406Arg
NM_001312675.1:c.*339G>A NP_001299604.1:n.*339G>A
NM_000504.4:c.1348G>A MANE Select NP_000495.1:p.Gly450Arg
NM_001312674.2:c.1216G>A NP_001299603.1:p.Gly406Arg
NM_001312675.2:c.*339G>A NP_001299604.1:n.*339G>A