Canonical Allele Identifier: CA388786768

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773135G>T (hg19) ; chr13:g.113118821G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118821G>T , CM000675.2:g.113118821G>T	GRCh38
NC_000013.10:g.113773135G>T , CM000675.1:g.113773135G>T	GRCh37
NC_000013.9:g.112821136G>T	NCBI36
NG_009258.1:g.1023G>T , LRG_548:g.1023G>T
NG_009262.1:g.18031G>T , LRG_554:g.18031G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1148G>T MANE Select	ENSP00000329546.4:p.Gly383Val
ENST00000346342.7:c.1148G>T	ENSP00000329546.3:p.Gly383Val
ENST00000375581.3:c.1214G>T	ENSP00000364731.3:p.Gly405Val
ENST00000541084.5:c.962G>T	ENSP00000442051.2:p.Gly321Val
NM_000131.4:c.1214G>T , LRG_554t1:c.1214G>T	NP_000122.1:p.Gly405Val
NM_001267554.1:c.962G>T	NP_001254483.1:p.Gly321Val
NM_019616.3:c.1148G>T , LRG_554t2:c.1148G>T	NP_062562.1:p.Gly383Val
NR_051961.1:n.1235G>T
XM_006719963.2:c.1007G>T	XP_006720026.1:p.Gly336Val
XM_011537474.1:c.1256G>T	XP_011535776.1:p.Gly419Val
XM_011537475.1:c.1070G>T	XP_011535777.1:p.Gly357Val
XM_011537476.1:c.908G>T	XP_011535778.1:p.Gly303Val
XM_011537477.1:c.1217G>T	XP_011535779.1:p.Gly406Val
XM_006719963.3:c.1052G>T	XP_006720026.2:p.Gly351Val
XM_011537474.2:c.1301G>T	XP_011535776.2:p.Gly434Val
XM_011537475.2:c.1115G>T	XP_011535777.2:p.Gly372Val
XM_011537476.2:c.908G>T	XP_011535778.1:p.Gly303Val
NM_019616.4:c.1148G>T MANE Select	NP_062562.1:p.Gly383Val
NR_051961.2:n.1232G>T
NM_001267554.2:c.962G>T	NP_001254483.1:p.Gly321Val