Canonical Allele Identifier: CA388785802

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772745A>G (hg19) ; chr13:g.113118431A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118431A>G , CM000675.2:g.113118431A>G	GRCh38
NC_000013.10:g.113772745A>G , CM000675.1:g.113772745A>G	GRCh37
NC_000013.9:g.112820746A>G	NCBI36
NG_009258.1:g.633A>G , LRG_548:g.633A>G
NG_009262.1:g.17641A>G , LRG_554:g.17641A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.758A>G MANE Select	ENSP00000329546.4:p.Glu253Gly
ENST00000346342.7:c.758A>G	ENSP00000329546.3:p.Glu253Gly
ENST00000375581.3:c.824A>G	ENSP00000364731.3:p.Glu275Gly
ENST00000541084.5:c.572A>G	ENSP00000442051.2:p.Glu191Gly
NM_000131.4:c.824A>G , LRG_554t1:c.824A>G	NP_000122.1:p.Glu275Gly
NM_001267554.1:c.572A>G	NP_001254483.1:p.Glu191Gly
NM_019616.3:c.758A>G , LRG_554t2:c.758A>G	NP_062562.1:p.Glu253Gly
NR_051961.1:n.845A>G
XM_006719963.2:c.617A>G	XP_006720026.1:p.Glu206Gly
XM_011537474.1:c.866A>G	XP_011535776.1:p.Glu289Gly
XM_011537475.1:c.680A>G	XP_011535777.1:p.Glu227Gly
XM_011537476.1:c.518A>G	XP_011535778.1:p.Glu173Gly
XM_011537477.1:c.827A>G	XP_011535779.1:p.Glu276Gly
XM_006719963.3:c.662A>G	XP_006720026.2:p.Glu221Gly
XM_011537474.2:c.911A>G	XP_011535776.2:p.Glu304Gly
XM_011537475.2:c.725A>G	XP_011535777.2:p.Glu242Gly
XM_011537476.2:c.518A>G	XP_011535778.1:p.Glu173Gly
NM_019616.4:c.758A>G MANE Select	NP_062562.1:p.Glu253Gly
NR_051961.2:n.842A>G
NM_001267554.2:c.572A>G	NP_001254483.1:p.Glu191Gly