Canonical Allele Identifier: CA388786560

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773093G>T (hg19) ; chr13:g.113118779G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118779G>T , CM000675.2:g.113118779G>T	GRCh38
NC_000013.10:g.113773093G>T , CM000675.1:g.113773093G>T	GRCh37
NC_000013.9:g.112821094G>T	NCBI36
NG_009258.1:g.981G>T , LRG_548:g.981G>T
NG_009262.1:g.17989G>T , LRG_554:g.17989G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1106G>T MANE Select	ENSP00000329546.4:p.Gly369Val
ENST00000346342.7:c.1106G>T	ENSP00000329546.3:p.Gly369Val
ENST00000375581.3:c.1172G>T	ENSP00000364731.3:p.Gly391Val
ENST00000541084.5:c.920G>T	ENSP00000442051.2:p.Gly307Val
NM_000131.4:c.1172G>T , LRG_554t1:c.1172G>T	NP_000122.1:p.Gly391Val
NM_001267554.1:c.920G>T	NP_001254483.1:p.Gly307Val
NM_019616.3:c.1106G>T , LRG_554t2:c.1106G>T	NP_062562.1:p.Gly369Val
NR_051961.1:n.1193G>T
XM_006719963.2:c.965G>T	XP_006720026.1:p.Gly322Val
XM_011537474.1:c.1214G>T	XP_011535776.1:p.Gly405Val
XM_011537475.1:c.1028G>T	XP_011535777.1:p.Gly343Val
XM_011537476.1:c.866G>T	XP_011535778.1:p.Gly289Val
XM_011537477.1:c.1175G>T	XP_011535779.1:p.Gly392Val
XM_006719963.3:c.1010G>T	XP_006720026.2:p.Gly337Val
XM_011537474.2:c.1259G>T	XP_011535776.2:p.Gly420Val
XM_011537475.2:c.1073G>T	XP_011535777.2:p.Gly358Val
XM_011537476.2:c.866G>T	XP_011535778.1:p.Gly289Val
NM_019616.4:c.1106G>T MANE Select	NP_062562.1:p.Gly369Val
NR_051961.2:n.1190G>T
NM_001267554.2:c.920G>T	NP_001254483.1:p.Gly307Val