Canonical Allele Identifier: CA2120140779

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149447T= , CM000675.2:g.113149447T=	GRCh38
NC_000013.10:g.113803761T= , CM000675.1:g.113803761T=	GRCh37
NC_000013.9:g.112851762T=	NCBI36
NG_009258.1:g.31649T= , LRG_548:g.31649T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1397T= MANE Select	ENSP00000364709.3:p.Met466=
ENST00000375551.7:c.*388T=	ENSP00000364701.3:n.*388T=
ENST00000375559.7:c.1397T=	ENSP00000364709.3:p.Met466=
ENST00000409306.5:c.*388T=	ENSP00000387092.1:n.*388T=
NM_000504.3:c.1397T= , LRG_548t1:c.1397T=	NP_000495.1:p.Met466=
NM_001312674.1:c.1265T=	NP_001299603.1:p.Met422=
NM_001312675.1:c.*388T=	NP_001299604.1:n.*388T=
NM_000504.4:c.1397T= MANE Select	NP_000495.1:p.Met466=
NM_001312674.2:c.1265T=	NP_001299603.1:p.Met422=
NM_001312675.2:c.*388T=	NP_001299604.1:n.*388T=