Canonical Allele Identifier: CA7060633

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113148952C>T , CM000675.2:g.113148952C>T	GRCh38
NC_000013.10:g.113803266C>T , CM000675.1:g.113803266C>T	GRCh37
NC_000013.9:g.112851267C>T	NCBI36
NG_009258.1:g.31154C>T , LRG_548:g.31154C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.902C>T MANE Select	ENSP00000364709.3:p.Ala301Val
ENST00000375551.7:c.892C>T	ENSP00000364701.3:p.Arg298Trp
ENST00000375559.7:c.902C>T	ENSP00000364709.3:p.Ala301Val
ENST00000409306.5:c.898C>T	ENSP00000387092.1:p.Arg300Trp
NM_000504.3:c.902C>T , LRG_548t1:c.902C>T	NP_000495.1:p.Ala301Val
NM_001312674.1:c.770C>T	NP_001299603.1:p.Ala257Val
NM_001312675.1:c.892C>T	NP_001299604.1:p.Arg298Trp
NM_000504.4:c.902C>T MANE Select	NP_000495.1:p.Ala301Val
NM_001312674.2:c.770C>T	NP_001299603.1:p.Ala257Val
NM_001312675.2:c.892C>T	NP_001299604.1:p.Arg298Trp