Canonical Allele Identifier: CA2018007878

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113140947C= , CM000675.2:g.113140947C=	GRCh38
NC_000013.10:g.113795261C= , CM000675.1:g.113795261C=	GRCh37
NC_000013.9:g.112843262C=	NCBI36
NG_009258.1:g.23149C= , LRG_548:g.23149C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000504.4:c.399C= MANE Select	NP_000495.1:p.Asn133=
ENST00000375559.8:c.399C= MANE Select	ENSP00000364709.3:p.Asn133=
NM_000504.3:c.399C= , LRG_548t1:c.399C=	NP_000495.1:p.Asn133=
NM_001312674.1:c.370+1477C=	NP_001299603.1:n.370+1477C=
NM_001312674.2:c.370+1477C=	NP_001299603.1:n.370+1477C=
NM_001312675.1:c.399C=	NP_001299604.1:p.Asn133=
NM_001312675.2:c.399C=	NP_001299604.1:p.Asn133=
ENST00000375551.7:c.399C=	ENSP00000364701.3:p.Asn133=
ENST00000375559.7:c.399C=	ENSP00000364709.3:p.Asn133=
ENST00000409306.5:c.399C=	ENSP00000387092.1:p.Asn133=
ENST00000410083.6:c.*358C=	ENSP00000386320.2:n.*358C=
ENST00000477269.5:n.436C=
ENST00000498455.1:n.428C=