Canonical Allele Identifier: CA2120143048

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118969G= , CM000675.2:g.113118969G=	GRCh38
NC_000013.10:g.113773283G= , CM000675.1:g.113773283G=	GRCh37
NC_000013.9:g.112821284G=	NCBI36
NG_009258.1:g.1171G= , LRG_548:g.1171G=
NG_009262.1:g.18179G= , LRG_554:g.18179G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1296G= MANE Select	ENSP00000329546.4:p.Glu432=
ENST00000346342.7:c.1296G=	ENSP00000329546.3:p.Glu432=
ENST00000375581.3:c.1362G=	ENSP00000364731.3:p.Glu454=
ENST00000541084.5:c.1110G=	ENSP00000442051.2:p.Glu370=
NM_000131.4:c.1362G= , LRG_554t1:c.1362G=	NP_000122.1:p.Glu454=
NM_001267554.1:c.1110G=	NP_001254483.1:p.Glu370=
NM_019616.3:c.1296G= , LRG_554t2:c.1296G=	NP_062562.1:p.Glu432=
NR_051961.1:n.1383G=
XM_006719963.2:c.1155G=	XP_006720026.1:p.Glu385=
XM_011537474.1:c.1404G=	XP_011535776.1:p.Glu468=
XM_011537475.1:c.1218G=	XP_011535777.1:p.Glu406=
XM_011537476.1:c.1056G=	XP_011535778.1:p.Glu352=
XM_011537477.1:c.1365G=	XP_011535779.1:p.Glu455=
XM_006719963.3:c.1200G=	XP_006720026.2:p.Glu400=
XM_011537474.2:c.1449G=	XP_011535776.2:p.Glu483=
XM_011537475.2:c.1263G=	XP_011535777.2:p.Glu421=
XM_011537476.2:c.1056G=	XP_011535778.1:p.Glu352=
NM_019616.4:c.1296G= MANE Select	NP_062562.1:p.Glu432=
NR_051961.2:n.1380G=
NM_001267554.2:c.1110G=	NP_001254483.1:p.Glu370=