Canonical Allele Identifier: CA388791194

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113147460T>A , CM000675.2:g.113147460T>A	GRCh38
NC_000013.10:g.113801774T>A , CM000675.1:g.113801774T>A	GRCh37
NC_000013.9:g.112849775T>A	NCBI36
NG_009258.1:g.29662T>A , LRG_548:g.29662T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000504.4:c.829T>A MANE Select	NP_000495.1:p.Cys277Ser
ENST00000375559.8:c.829T>A MANE Select	ENSP00000364709.3:p.Cys277Ser
NM_000504.3:c.829T>A , LRG_548t1:c.829T>A	NP_000495.1:p.Cys277Ser
NM_001312674.1:c.697T>A	NP_001299603.1:p.Cys233Ser
NM_001312674.2:c.697T>A	NP_001299603.1:p.Cys233Ser
NM_001312675.1:c.829T>A	NP_001299604.1:p.Cys277Ser
NM_001312675.2:c.829T>A	NP_001299604.1:p.Cys277Ser
ENST00000375551.7:c.829T>A	ENSP00000364701.3:p.Cys277Ser
ENST00000375559.7:c.829T>A	ENSP00000364709.3:p.Cys277Ser
ENST00000409306.5:c.829T>A	ENSP00000387092.1:p.Cys277Ser
ENST00000410083.6:c.*788T>A	ENSP00000386320.2:n.*788T>A