Canonical Allele Identifier: CA485021196

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773136A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118822A>G , CM000675.2:g.113118822A>G	GRCh38
NC_000013.10:g.113773136A>G , CM000675.1:g.113773136A>G	GRCh37
NC_000013.9:g.112821137A>G	NCBI36
NG_009258.1:g.1024A>G , LRG_548:g.1024A>G
NG_009262.1:g.18032A>G , LRG_554:g.18032A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1149A>G MANE Select	ENSP00000329546.4:p.Gly383=
ENST00000346342.7:c.1149A>G	ENSP00000329546.3:p.Gly383=
ENST00000375581.3:c.1215A>G	ENSP00000364731.3:p.Gly405=
ENST00000541084.5:c.963A>G	ENSP00000442051.2:p.Gly321=
NM_000131.4:c.1215A>G , LRG_554t1:c.1215A>G	NP_000122.1:p.Gly405=
NM_001267554.1:c.963A>G	NP_001254483.1:p.Gly321=
NM_019616.3:c.1149A>G , LRG_554t2:c.1149A>G	NP_062562.1:p.Gly383=
NR_051961.1:n.1236A>G
XM_006719963.2:c.1008A>G	XP_006720026.1:p.Gly336=
XM_011537474.1:c.1257A>G	XP_011535776.1:p.Gly419=
XM_011537475.1:c.1071A>G	XP_011535777.1:p.Gly357=
XM_011537476.1:c.909A>G	XP_011535778.1:p.Gly303=
XM_011537477.1:c.1218A>G	XP_011535779.1:p.Gly406=
XM_006719963.3:c.1053A>G	XP_006720026.2:p.Gly351=
XM_011537474.2:c.1302A>G	XP_011535776.2:p.Gly434=
XM_011537475.2:c.1116A>G	XP_011535777.2:p.Gly372=
XM_011537476.2:c.909A>G	XP_011535778.1:p.Gly303=
NM_019616.4:c.1149A>G MANE Select	NP_062562.1:p.Gly383=
NR_051961.2:n.1233A>G
NM_001267554.2:c.963A>G	NP_001254483.1:p.Gly321=