Canonical Allele Identifier: CA388786755

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773133T>G (hg19) ; chr13:g.113118819T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118819T>G , CM000675.2:g.113118819T>G	GRCh38
NC_000013.10:g.113773133T>G , CM000675.1:g.113773133T>G	GRCh37
NC_000013.9:g.112821134T>G	NCBI36
NG_009258.1:g.1021T>G , LRG_548:g.1021T>G
NG_009262.1:g.18029T>G , LRG_554:g.18029T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1146T>G MANE Select	ENSP00000329546.4:p.Ser382Arg
ENST00000346342.7:c.1146T>G	ENSP00000329546.3:p.Ser382Arg
ENST00000375581.3:c.1212T>G	ENSP00000364731.3:p.Ser404Arg
ENST00000541084.5:c.960T>G	ENSP00000442051.2:p.Ser320Arg
NM_000131.4:c.1212T>G , LRG_554t1:c.1212T>G	NP_000122.1:p.Ser404Arg
NM_001267554.1:c.960T>G	NP_001254483.1:p.Ser320Arg
NM_019616.3:c.1146T>G , LRG_554t2:c.1146T>G	NP_062562.1:p.Ser382Arg
NR_051961.1:n.1233T>G
XM_006719963.2:c.1005T>G	XP_006720026.1:p.Ser335Arg
XM_011537474.1:c.1254T>G	XP_011535776.1:p.Ser418Arg
XM_011537475.1:c.1068T>G	XP_011535777.1:p.Ser356Arg
XM_011537476.1:c.906T>G	XP_011535778.1:p.Ser302Arg
XM_011537477.1:c.1215T>G	XP_011535779.1:p.Ser405Arg
XM_006719963.3:c.1050T>G	XP_006720026.2:p.Ser350Arg
XM_011537474.2:c.1299T>G	XP_011535776.2:p.Ser433Arg
XM_011537475.2:c.1113T>G	XP_011535777.2:p.Ser371Arg
XM_011537476.2:c.906T>G	XP_011535778.1:p.Ser302Arg
NM_019616.4:c.1146T>G MANE Select	NP_062562.1:p.Ser382Arg
NR_051961.2:n.1230T>G
NM_001267554.2:c.960T>G	NP_001254483.1:p.Ser320Arg