Canonical Allele Identifier: CA388785937

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772814C>G (hg19) ; chr13:g.113118500C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118500C>G , CM000675.2:g.113118500C>G	GRCh38
NC_000013.10:g.113772814C>G , CM000675.1:g.113772814C>G	GRCh37
NC_000013.9:g.112820815C>G	NCBI36
NG_009258.1:g.702C>G , LRG_548:g.702C>G
NG_009262.1:g.17710C>G , LRG_554:g.17710C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.827C>G MANE Select	ENSP00000329546.4:p.Thr276Ser
ENST00000346342.7:c.827C>G	ENSP00000329546.3:p.Thr276Ser
ENST00000375581.3:c.893C>G	ENSP00000364731.3:p.Thr298Ser
ENST00000541084.5:c.641C>G	ENSP00000442051.2:p.Thr214Ser
NM_000131.4:c.893C>G , LRG_554t1:c.893C>G	NP_000122.1:p.Thr298Ser
NM_001267554.1:c.641C>G	NP_001254483.1:p.Thr214Ser
NM_019616.3:c.827C>G , LRG_554t2:c.827C>G	NP_062562.1:p.Thr276Ser
NR_051961.1:n.914C>G
XM_006719963.2:c.686C>G	XP_006720026.1:p.Thr229Ser
XM_011537474.1:c.935C>G	XP_011535776.1:p.Thr312Ser
XM_011537475.1:c.749C>G	XP_011535777.1:p.Thr250Ser
XM_011537476.1:c.587C>G	XP_011535778.1:p.Thr196Ser
XM_011537477.1:c.896C>G	XP_011535779.1:p.Thr299Ser
XM_006719963.3:c.731C>G	XP_006720026.2:p.Thr244Ser
XM_011537474.2:c.980C>G	XP_011535776.2:p.Thr327Ser
XM_011537475.2:c.794C>G	XP_011535777.2:p.Thr265Ser
XM_011537476.2:c.587C>G	XP_011535778.1:p.Thr196Ser
NM_019616.4:c.827C>G MANE Select	NP_062562.1:p.Thr276Ser
NR_051961.2:n.911C>G
NM_001267554.2:c.641C>G	NP_001254483.1:p.Thr214Ser