Canonical Allele Identifier: CA2120142039

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118541G= , CM000675.2:g.113118541G=	GRCh38
NC_000013.10:g.113772855G= , CM000675.1:g.113772855G=	GRCh37
NC_000013.9:g.112820856G=	NCBI36
NG_009258.1:g.743G= , LRG_548:g.743G=
NG_009262.1:g.17751G= , LRG_554:g.17751G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.868G= MANE Select	ENSP00000329546.4:p.Val290=
ENST00000346342.7:c.868G=	ENSP00000329546.3:p.Val290=
ENST00000375581.3:c.934G=	ENSP00000364731.3:p.Val312=
ENST00000541084.5:c.682G=	ENSP00000442051.2:p.Val228=
NM_000131.4:c.934G= , LRG_554t1:c.934G=	NP_000122.1:p.Val312=
NM_001267554.1:c.682G=	NP_001254483.1:p.Val228=
NM_019616.3:c.868G= , LRG_554t2:c.868G=	NP_062562.1:p.Val290=
NR_051961.1:n.955G=
XM_006719963.2:c.727G=	XP_006720026.1:p.Val243=
XM_011537474.1:c.976G=	XP_011535776.1:p.Val326=
XM_011537475.1:c.790G=	XP_011535777.1:p.Val264=
XM_011537476.1:c.628G=	XP_011535778.1:p.Val210=
XM_011537477.1:c.937G=	XP_011535779.1:p.Val313=
XM_006719963.3:c.772G=	XP_006720026.2:p.Val258=
XM_011537474.2:c.1021G=	XP_011535776.2:p.Val341=
XM_011537475.2:c.835G=	XP_011535777.2:p.Val279=
XM_011537476.2:c.628G=	XP_011535778.1:p.Val210=
NM_019616.4:c.868G= MANE Select	NP_062562.1:p.Val290=
NR_051961.2:n.952G=
NM_001267554.2:c.682G=	NP_001254483.1:p.Val228=