Canonical Allele Identifier: CA388782504

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768263A>G (hg19) ; chr13:g.113113949A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113949A>G , CM000675.2:g.113113949A>G	GRCh38
NC_000013.10:g.113768263A>G , CM000675.1:g.113768263A>G	GRCh37
NC_000013.9:g.112816264A>G	NCBI36
NG_009262.1:g.13159A>G , LRG_554:g.13159A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.353A>G MANE Select	ENSP00000329546.4:p.Asn118Ser
ENST00000346342.7:c.353A>G	ENSP00000329546.3:p.Asn118Ser
ENST00000375581.3:c.419A>G	ENSP00000364731.3:p.Asn140Ser
ENST00000444337.1:c.*161A>G	ENSP00000387669.1:n.*161A>G
ENST00000473085.1:n.300A>G
ENST00000479674.1:n.686A>G
ENST00000541084.5:c.167A>G	ENSP00000442051.2:p.Asn56Ser
NM_000131.4:c.419A>G , LRG_554t1:c.419A>G	NP_000122.1:p.Asn140Ser
NM_001267554.1:c.167A>G	NP_001254483.1:p.Asn56Ser
NM_019616.3:c.353A>G , LRG_554t2:c.353A>G	NP_062562.1:p.Asn118Ser
NR_051961.1:n.440A>G
XM_006719963.2:c.353A>G	XP_006720026.1:p.Asn118Ser
XM_011537474.1:c.353A>G	XP_011535776.1:p.Asn118Ser
XM_011537475.1:c.167A>G	XP_011535777.1:p.Asn56Ser
XM_011537477.1:c.314A>G	XP_011535779.1:p.Asn105Ser
XM_006719963.3:c.398A>G	XP_006720026.2:p.Asn133Ser
XM_011537474.2:c.398A>G	XP_011535776.2:p.Asn133Ser
XM_011537475.2:c.212A>G	XP_011535777.2:p.Asn71Ser
NM_019616.4:c.353A>G MANE Select	NP_062562.1:p.Asn118Ser
NR_051961.2:n.437A>G
NM_001267554.2:c.167A>G	NP_001254483.1:p.Asn56Ser