Canonical Allele Identifier: CA388786469

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773074G>T (hg19) ; chr13:g.113118760G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118760G>T , CM000675.2:g.113118760G>T	GRCh38
NC_000013.10:g.113773074G>T , CM000675.1:g.113773074G>T	GRCh37
NC_000013.9:g.112821075G>T	NCBI36
NG_009258.1:g.962G>T , LRG_548:g.962G>T
NG_009262.1:g.17970G>T , LRG_554:g.17970G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1087G>T MANE Select	ENSP00000329546.4:p.Glu363Ter
ENST00000346342.7:c.1087G>T	ENSP00000329546.3:p.Glu363Ter
ENST00000375581.3:c.1153G>T	ENSP00000364731.3:p.Glu385Ter
ENST00000541084.5:c.901G>T	ENSP00000442051.2:p.Glu301Ter
NM_000131.4:c.1153G>T , LRG_554t1:c.1153G>T	NP_000122.1:p.Glu385Ter
NM_001267554.1:c.901G>T	NP_001254483.1:p.Glu301Ter
NM_019616.3:c.1087G>T , LRG_554t2:c.1087G>T	NP_062562.1:p.Glu363Ter
NR_051961.1:n.1174G>T
XM_006719963.2:c.946G>T	XP_006720026.1:p.Glu316Ter
XM_011537474.1:c.1195G>T	XP_011535776.1:p.Glu399Ter
XM_011537475.1:c.1009G>T	XP_011535777.1:p.Glu337Ter
XM_011537476.1:c.847G>T	XP_011535778.1:p.Glu283Ter
XM_011537477.1:c.1156G>T	XP_011535779.1:p.Glu386Ter
XM_006719963.3:c.991G>T	XP_006720026.2:p.Glu331Ter
XM_011537474.2:c.1240G>T	XP_011535776.2:p.Glu414Ter
XM_011537475.2:c.1054G>T	XP_011535777.2:p.Glu352Ter
XM_011537476.2:c.847G>T	XP_011535778.1:p.Glu283Ter
NM_019616.4:c.1087G>T MANE Select	NP_062562.1:p.Glu363Ter
NR_051961.2:n.1171G>T
NM_001267554.2:c.901G>T	NP_001254483.1:p.Glu301Ter