Canonical Allele Identifier: CA485423881

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772842C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118528C>G , CM000675.2:g.113118528C>G	GRCh38
NC_000013.10:g.113772842C>G , CM000675.1:g.113772842C>G	GRCh37
NC_000013.9:g.112820843C>G	NCBI36
NG_009258.1:g.730C>G , LRG_548:g.730C>G
NG_009262.1:g.17738C>G , LRG_554:g.17738C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.855C>G MANE Select	ENSP00000329546.4:p.Arg285=
ENST00000346342.7:c.855C>G	ENSP00000329546.3:p.Arg285=
ENST00000375581.3:c.921C>G	ENSP00000364731.3:p.Arg307=
ENST00000541084.5:c.669C>G	ENSP00000442051.2:p.Arg223=
NM_000131.4:c.921C>G , LRG_554t1:c.921C>G	NP_000122.1:p.Arg307=
NM_001267554.1:c.669C>G	NP_001254483.1:p.Arg223=
NM_019616.3:c.855C>G , LRG_554t2:c.855C>G	NP_062562.1:p.Arg285=
NR_051961.1:n.942C>G
XM_006719963.2:c.714C>G	XP_006720026.1:p.Arg238=
XM_011537474.1:c.963C>G	XP_011535776.1:p.Arg321=
XM_011537475.1:c.777C>G	XP_011535777.1:p.Arg259=
XM_011537476.1:c.615C>G	XP_011535778.1:p.Arg205=
XM_011537477.1:c.924C>G	XP_011535779.1:p.Arg308=
XM_006719963.3:c.759C>G	XP_006720026.2:p.Arg253=
XM_011537474.2:c.1008C>G	XP_011535776.2:p.Arg336=
XM_011537475.2:c.822C>G	XP_011535777.2:p.Arg274=
XM_011537476.2:c.615C>G	XP_011535778.1:p.Arg205=
NM_019616.4:c.855C>G MANE Select	NP_062562.1:p.Arg285=
NR_051961.2:n.939C>G
NM_001267554.2:c.669C>G	NP_001254483.1:p.Arg223=