Canonical Allele Identifier: CA7060705
Gene: F10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1341356
ClinVar RCV Id: RCV001834560
dbSNP Id: rs376163818

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149266G>A , CM000675.2:g.113149266G>A GRCh38
NC_000013.10:g.113803580G>A , CM000675.1:g.113803580G>A GRCh37
NC_000013.9:g.112851581G>A NCBI36
NG_009258.1:g.31468G>A , LRG_548:g.31468G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1216G>A MANE Select ENSP00000364709.3:p.Gly406Ser
ENST00000375551.7:c.*207G>A ENSP00000364701.3:n.*207G>A
ENST00000375559.7:c.1216G>A ENSP00000364709.3:p.Gly406Ser
ENST00000409306.5:c.*207G>A ENSP00000387092.1:n.*207G>A
NM_000504.3:c.1216G>A , LRG_548t1:c.1216G>A NP_000495.1:p.Gly406Ser
NM_001312674.1:c.1084G>A NP_001299603.1:p.Gly362Ser
NM_001312675.1:c.*207G>A NP_001299604.1:n.*207G>A
NM_000504.4:c.1216G>A MANE Select NP_000495.1:p.Gly406Ser
NM_001312674.2:c.1084G>A NP_001299603.1:p.Gly362Ser
NM_001312675.2:c.*207G>A NP_001299604.1:n.*207G>A