Canonical Allele Identifier: CA2120140069

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149061C= , CM000675.2:g.113149061C=	GRCh38
NC_000013.10:g.113803375C= , CM000675.1:g.113803375C=	GRCh37
NC_000013.9:g.112851376C=	NCBI36
NG_009258.1:g.31263C= , LRG_548:g.31263C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.1011C= MANE Select	ENSP00000364709.3:p.Asn337=
ENST00000375551.7:c.*2C=	ENSP00000364701.3:n.*2C=
ENST00000375559.7:c.1011C=	ENSP00000364709.3:p.Asn337=
ENST00000409306.5:c.*2C=	ENSP00000387092.1:n.*2C=
NM_000504.3:c.1011C= , LRG_548t1:c.1011C=	NP_000495.1:p.Asn337=
NM_001312674.1:c.879C=	NP_001299603.1:p.Asn293=
NM_001312675.1:c.*2C=	NP_001299604.1:n.*2C=
NM_000504.4:c.1011C= MANE Select	NP_000495.1:p.Asn337=
NM_001312674.2:c.879C=	NP_001299603.1:p.Asn293=
NM_001312675.2:c.*2C=	NP_001299604.1:n.*2C=