Canonical Allele Identifier: CA388794522
Gene: F10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149442G>T , CM000675.2:g.113149442G>T GRCh38
NC_000013.10:g.113803756G>T , CM000675.1:g.113803756G>T GRCh37
NC_000013.9:g.112851757G>T NCBI36
NG_009258.1:g.31644G>T , LRG_548:g.31644G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1392G>T MANE Select ENSP00000364709.3:p.Arg464Ser
ENST00000375551.7:c.*383G>T ENSP00000364701.3:n.*383G>T
ENST00000375559.7:c.1392G>T ENSP00000364709.3:p.Arg464Ser
ENST00000409306.5:c.*383G>T ENSP00000387092.1:n.*383G>T
NM_000504.3:c.1392G>T , LRG_548t1:c.1392G>T NP_000495.1:p.Arg464Ser
NM_001312674.1:c.1260G>T NP_001299603.1:p.Arg420Ser
NM_001312675.1:c.*383G>T NP_001299604.1:n.*383G>T
NM_000504.4:c.1392G>T MANE Select NP_000495.1:p.Arg464Ser
NM_001312674.2:c.1260G>T NP_001299603.1:p.Arg420Ser
NM_001312675.2:c.*383G>T NP_001299604.1:n.*383G>T