Canonical Allele Identifier: CA485424006

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773022C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118708C>G , CM000675.2:g.113118708C>G	GRCh38
NC_000013.10:g.113773022C>G , CM000675.1:g.113773022C>G	GRCh37
NC_000013.9:g.112821023C>G	NCBI36
NG_009258.1:g.910C>G , LRG_548:g.910C>G
NG_009262.1:g.17918C>G , LRG_554:g.17918C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1035C>G MANE Select	ENSP00000329546.4:p.Thr345=
ENST00000346342.7:c.1035C>G	ENSP00000329546.3:p.Thr345=
ENST00000375581.3:c.1101C>G	ENSP00000364731.3:p.Thr367=
ENST00000541084.5:c.849C>G	ENSP00000442051.2:p.Thr283=
NM_000131.4:c.1101C>G , LRG_554t1:c.1101C>G	NP_000122.1:p.Thr367=
NM_001267554.1:c.849C>G	NP_001254483.1:p.Thr283=
NM_019616.3:c.1035C>G , LRG_554t2:c.1035C>G	NP_062562.1:p.Thr345=
NR_051961.1:n.1122C>G
XM_006719963.2:c.894C>G	XP_006720026.1:p.Thr298=
XM_011537474.1:c.1143C>G	XP_011535776.1:p.Thr381=
XM_011537475.1:c.957C>G	XP_011535777.1:p.Thr319=
XM_011537476.1:c.795C>G	XP_011535778.1:p.Thr265=
XM_011537477.1:c.1104C>G	XP_011535779.1:p.Thr368=
XM_006719963.3:c.939C>G	XP_006720026.2:p.Thr313=
XM_011537474.2:c.1188C>G	XP_011535776.2:p.Thr396=
XM_011537475.2:c.1002C>G	XP_011535777.2:p.Thr334=
XM_011537476.2:c.795C>G	XP_011535778.1:p.Thr265=
NM_019616.4:c.1035C>G MANE Select	NP_062562.1:p.Thr345=
NR_051961.2:n.1119C>G
NM_001267554.2:c.849C>G	NP_001254483.1:p.Thr283=