Canonical Allele Identifier: CA485020427

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768273G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113959G>T , CM000675.2:g.113113959G>T	GRCh38
NC_000013.10:g.113768273G>T , CM000675.1:g.113768273G>T	GRCh37
NC_000013.9:g.112816274G>T	NCBI36
NG_009262.1:g.13169G>T , LRG_554:g.13169G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.363G>T MANE Select	ENSP00000329546.4:p.Thr121=
ENST00000346342.7:c.363G>T	ENSP00000329546.3:p.Thr121=
ENST00000375581.3:c.429G>T	ENSP00000364731.3:p.Thr143=
ENST00000444337.1:c.*171G>T	ENSP00000387669.1:n.*171G>T
ENST00000473085.1:n.310G>T
ENST00000479674.1:n.696G>T
ENST00000541084.5:c.177G>T	ENSP00000442051.2:p.Thr59=
NM_000131.4:c.429G>T , LRG_554t1:c.429G>T	NP_000122.1:p.Thr143=
NM_001267554.1:c.177G>T	NP_001254483.1:p.Thr59=
NM_019616.3:c.363G>T , LRG_554t2:c.363G>T	NP_062562.1:p.Thr121=
NR_051961.1:n.450G>T
XM_006719963.2:c.363G>T	XP_006720026.1:p.Thr121=
XM_011537474.1:c.363G>T	XP_011535776.1:p.Thr121=
XM_011537475.1:c.177G>T	XP_011535777.1:p.Thr59=
XM_011537477.1:c.324G>T	XP_011535779.1:p.Thr108=
XM_006719963.3:c.408G>T	XP_006720026.2:p.Thr136=
XM_011537474.2:c.408G>T	XP_011535776.2:p.Thr136=
XM_011537475.2:c.222G>T	XP_011535777.2:p.Thr74=
NM_019616.4:c.363G>T MANE Select	NP_062562.1:p.Thr121=
NR_051961.2:n.447G>T
NM_001267554.2:c.177G>T	NP_001254483.1:p.Thr59=