Canonical Allele Identifier: CA485020418

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768264C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113950C>T , CM000675.2:g.113113950C>T	GRCh38
NC_000013.10:g.113768264C>T , CM000675.1:g.113768264C>T	GRCh37
NC_000013.9:g.112816265C>T	NCBI36
NG_009262.1:g.13160C>T , LRG_554:g.13160C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.354C>T MANE Select	ENSP00000329546.4:p.Asn118=
ENST00000346342.7:c.354C>T	ENSP00000329546.3:p.Asn118=
ENST00000375581.3:c.420C>T	ENSP00000364731.3:p.Asn140=
ENST00000444337.1:c.*162C>T	ENSP00000387669.1:n.*162C>T
ENST00000473085.1:n.301C>T
ENST00000479674.1:n.687C>T
ENST00000541084.5:c.168C>T	ENSP00000442051.2:p.Asn56=
NM_000131.4:c.420C>T , LRG_554t1:c.420C>T	NP_000122.1:p.Asn140=
NM_001267554.1:c.168C>T	NP_001254483.1:p.Asn56=
NM_019616.3:c.354C>T , LRG_554t2:c.354C>T	NP_062562.1:p.Asn118=
NR_051961.1:n.441C>T
XM_006719963.2:c.354C>T	XP_006720026.1:p.Asn118=
XM_011537474.1:c.354C>T	XP_011535776.1:p.Asn118=
XM_011537475.1:c.168C>T	XP_011535777.1:p.Asn56=
XM_011537477.1:c.315C>T	XP_011535779.1:p.Asn105=
XM_006719963.3:c.399C>T	XP_006720026.2:p.Asn133=
XM_011537474.2:c.399C>T	XP_011535776.2:p.Asn133=
XM_011537475.2:c.213C>T	XP_011535777.2:p.Asn71=
NM_019616.4:c.354C>T MANE Select	NP_062562.1:p.Asn118=
NR_051961.2:n.438C>T
NM_001267554.2:c.168C>T	NP_001254483.1:p.Asn56=