Canonical Allele Identifier: CA388786424

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773060C>G (hg19) ; chr13:g.113118746C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118746C>G , CM000675.2:g.113118746C>G	GRCh38
NC_000013.10:g.113773060C>G , CM000675.1:g.113773060C>G	GRCh37
NC_000013.9:g.112821061C>G	NCBI36
NG_009258.1:g.948C>G , LRG_548:g.948C>G
NG_009262.1:g.17956C>G , LRG_554:g.17956C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1073C>G MANE Select	ENSP00000329546.4:p.Ser358Cys
ENST00000346342.7:c.1073C>G	ENSP00000329546.3:p.Ser358Cys
ENST00000375581.3:c.1139C>G	ENSP00000364731.3:p.Ser380Cys
ENST00000541084.5:c.887C>G	ENSP00000442051.2:p.Ser296Cys
NM_000131.4:c.1139C>G , LRG_554t1:c.1139C>G	NP_000122.1:p.Ser380Cys
NM_001267554.1:c.887C>G	NP_001254483.1:p.Ser296Cys
NM_019616.3:c.1073C>G , LRG_554t2:c.1073C>G	NP_062562.1:p.Ser358Cys
NR_051961.1:n.1160C>G
XM_006719963.2:c.932C>G	XP_006720026.1:p.Ser311Cys
XM_011537474.1:c.1181C>G	XP_011535776.1:p.Ser394Cys
XM_011537475.1:c.995C>G	XP_011535777.1:p.Ser332Cys
XM_011537476.1:c.833C>G	XP_011535778.1:p.Ser278Cys
XM_011537477.1:c.1142C>G	XP_011535779.1:p.Ser381Cys
XM_006719963.3:c.977C>G	XP_006720026.2:p.Ser326Cys
XM_011537474.2:c.1226C>G	XP_011535776.2:p.Ser409Cys
XM_011537475.2:c.1040C>G	XP_011535777.2:p.Ser347Cys
XM_011537476.2:c.833C>G	XP_011535778.1:p.Ser278Cys
NM_019616.4:c.1073C>G MANE Select	NP_062562.1:p.Ser358Cys
NR_051961.2:n.1157C>G
NM_001267554.2:c.887C>G	NP_001254483.1:p.Ser296Cys