Canonical Allele Identifier: CA388794426
Gene: F10 HGNC NCBI

Linked Data

dbSNP Id: rs777379687

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149419G>T , CM000675.2:g.113149419G>T GRCh38
NC_000013.10:g.113803733G>T , CM000675.1:g.113803733G>T GRCh37
NC_000013.9:g.112851734G>T NCBI36
NG_009258.1:g.31621G>T , LRG_548:g.31621G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1369G>T MANE Select ENSP00000364709.3:p.Ala457Ser
ENST00000375551.7:c.*360G>T ENSP00000364701.3:n.*360G>T
ENST00000375559.7:c.1369G>T ENSP00000364709.3:p.Ala457Ser
ENST00000409306.5:c.*360G>T ENSP00000387092.1:n.*360G>T
NM_000504.3:c.1369G>T , LRG_548t1:c.1369G>T NP_000495.1:p.Ala457Ser
NM_001312674.1:c.1237G>T NP_001299603.1:p.Ala413Ser
NM_001312675.1:c.*360G>T NP_001299604.1:n.*360G>T
NM_000504.4:c.1369G>T MANE Select NP_000495.1:p.Ala457Ser
NM_001312674.2:c.1237G>T NP_001299603.1:p.Ala413Ser
NM_001312675.2:c.*360G>T NP_001299604.1:n.*360G>T