Canonical Allele Identifier: CA2120135657

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113929C= , CM000675.2:g.113113929C=	GRCh38
NC_000013.10:g.113768243C= , CM000675.1:g.113768243C=	GRCh37
NC_000013.9:g.112816244C=	NCBI36
NG_009262.1:g.13139C= , LRG_554:g.13139C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.333C= MANE Select	ENSP00000329546.4:p.Leu111=
ENST00000346342.7:c.333C=	ENSP00000329546.3:p.Leu111=
ENST00000375581.3:c.399C=	ENSP00000364731.3:p.Leu133=
ENST00000444337.1:c.*141C=	ENSP00000387669.1:n.*141C=
ENST00000473085.1:n.280C=
ENST00000479674.1:n.666C=
ENST00000541084.5:c.147C=	ENSP00000442051.2:p.Leu49=
NM_000131.4:c.399C= , LRG_554t1:c.399C=	NP_000122.1:p.Leu133=
NM_001267554.1:c.147C=	NP_001254483.1:p.Leu49=
NM_019616.3:c.333C= , LRG_554t2:c.333C=	NP_062562.1:p.Leu111=
NR_051961.1:n.420C=
XM_006719963.2:c.333C=	XP_006720026.1:p.Leu111=
XM_011537474.1:c.333C=	XP_011535776.1:p.Leu111=
XM_011537475.1:c.147C=	XP_011535777.1:p.Leu49=
XM_011537477.1:c.294C=	XP_011535779.1:p.Leu98=
XM_006719963.3:c.378C=	XP_006720026.2:p.Leu126=
XM_011537474.2:c.378C=	XP_011535776.2:p.Leu126=
XM_011537475.2:c.192C=	XP_011535777.2:p.Leu64=
NM_019616.4:c.333C= MANE Select	NP_062562.1:p.Leu111=
NR_051961.2:n.417C=
NM_001267554.2:c.147C=	NP_001254483.1:p.Leu49=