Canonical Allele Identifier: CA388785852

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772767C>G (hg19) ; chr13:g.113118453C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118453C>G , CM000675.2:g.113118453C>G	GRCh38
NC_000013.10:g.113772767C>G , CM000675.1:g.113772767C>G	GRCh37
NC_000013.9:g.112820768C>G	NCBI36
NG_009258.1:g.655C>G , LRG_548:g.655C>G
NG_009262.1:g.17663C>G , LRG_554:g.17663C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.780C>G MANE Select	ENSP00000329546.4:p.Ser260Arg
ENST00000346342.7:c.780C>G	ENSP00000329546.3:p.Ser260Arg
ENST00000375581.3:c.846C>G	ENSP00000364731.3:p.Ser282Arg
ENST00000541084.5:c.594C>G	ENSP00000442051.2:p.Ser198Arg
NM_000131.4:c.846C>G , LRG_554t1:c.846C>G	NP_000122.1:p.Ser282Arg
NM_001267554.1:c.594C>G	NP_001254483.1:p.Ser198Arg
NM_019616.3:c.780C>G , LRG_554t2:c.780C>G	NP_062562.1:p.Ser260Arg
NR_051961.1:n.867C>G
XM_006719963.2:c.639C>G	XP_006720026.1:p.Ser213Arg
XM_011537474.1:c.888C>G	XP_011535776.1:p.Ser296Arg
XM_011537475.1:c.702C>G	XP_011535777.1:p.Ser234Arg
XM_011537476.1:c.540C>G	XP_011535778.1:p.Ser180Arg
XM_011537477.1:c.849C>G	XP_011535779.1:p.Ser283Arg
XM_006719963.3:c.684C>G	XP_006720026.2:p.Ser228Arg
XM_011537474.2:c.933C>G	XP_011535776.2:p.Ser311Arg
XM_011537475.2:c.747C>G	XP_011535777.2:p.Ser249Arg
XM_011537476.2:c.540C>G	XP_011535778.1:p.Ser180Arg
NM_019616.4:c.780C>G MANE Select	NP_062562.1:p.Ser260Arg
NR_051961.2:n.864C>G
NM_001267554.2:c.594C>G	NP_001254483.1:p.Ser198Arg