Canonical Allele Identifier: CA388785991

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772843C>A (hg19) ; chr13:g.113118529C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118529C>A , CM000675.2:g.113118529C>A	GRCh38
NC_000013.10:g.113772843C>A , CM000675.1:g.113772843C>A	GRCh37
NC_000013.9:g.112820844C>A	NCBI36
NG_009258.1:g.731C>A , LRG_548:g.731C>A
NG_009262.1:g.17739C>A , LRG_554:g.17739C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.856C>A MANE Select	ENSP00000329546.4:p.Leu286Met
ENST00000346342.7:c.856C>A	ENSP00000329546.3:p.Leu286Met
ENST00000375581.3:c.922C>A	ENSP00000364731.3:p.Leu308Met
ENST00000541084.5:c.670C>A	ENSP00000442051.2:p.Leu224Met
NM_000131.4:c.922C>A , LRG_554t1:c.922C>A	NP_000122.1:p.Leu308Met
NM_001267554.1:c.670C>A	NP_001254483.1:p.Leu224Met
NM_019616.3:c.856C>A , LRG_554t2:c.856C>A	NP_062562.1:p.Leu286Met
NR_051961.1:n.943C>A
XM_006719963.2:c.715C>A	XP_006720026.1:p.Leu239Met
XM_011537474.1:c.964C>A	XP_011535776.1:p.Leu322Met
XM_011537475.1:c.778C>A	XP_011535777.1:p.Leu260Met
XM_011537476.1:c.616C>A	XP_011535778.1:p.Leu206Met
XM_011537477.1:c.925C>A	XP_011535779.1:p.Leu309Met
XM_006719963.3:c.760C>A	XP_006720026.2:p.Leu254Met
XM_011537474.2:c.1009C>A	XP_011535776.2:p.Leu337Met
XM_011537475.2:c.823C>A	XP_011535777.2:p.Leu275Met
XM_011537476.2:c.616C>A	XP_011535778.1:p.Leu206Met
NM_019616.4:c.856C>A MANE Select	NP_062562.1:p.Leu286Met
NR_051961.2:n.940C>A
NM_001267554.2:c.670C>A	NP_001254483.1:p.Leu224Met