Canonical Allele Identifier: CA2120140487

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149325C= , CM000675.2:g.113149325C=	GRCh38
NC_000013.10:g.113803639C= , CM000675.1:g.113803639C=	GRCh37
NC_000013.9:g.112851640C=	NCBI36
NG_009258.1:g.31527C= , LRG_548:g.31527C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1275C= MANE Select	ENSP00000364709.3:p.Thr425=
ENST00000375551.7:c.*266C=	ENSP00000364701.3:n.*266C=
ENST00000375559.7:c.1275C=	ENSP00000364709.3:p.Thr425=
ENST00000409306.5:c.*266C=	ENSP00000387092.1:n.*266C=
NM_000504.3:c.1275C= , LRG_548t1:c.1275C=	NP_000495.1:p.Thr425=
NM_001312674.1:c.1143C=	NP_001299603.1:p.Thr381=
NM_001312675.1:c.*266C=	NP_001299604.1:n.*266C=
NM_000504.4:c.1275C= MANE Select	NP_000495.1:p.Thr425=
NM_001312674.2:c.1143C=	NP_001299603.1:p.Thr381=
NM_001312675.2:c.*266C=	NP_001299604.1:n.*266C=