Canonical Allele Identifier: CA388782465

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768254A>T (hg19) ; chr13:g.113113940A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113940A>T , CM000675.2:g.113113940A>T	GRCh38
NC_000013.10:g.113768254A>T , CM000675.1:g.113768254A>T	GRCh37
NC_000013.9:g.112816255A>T	NCBI36
NG_009262.1:g.13150A>T , LRG_554:g.13150A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.344A>T MANE Select	ENSP00000329546.4:p.Glu115Val
ENST00000346342.7:c.344A>T	ENSP00000329546.3:p.Glu115Val
ENST00000375581.3:c.410A>T	ENSP00000364731.3:p.Glu137Val
ENST00000444337.1:c.*152A>T	ENSP00000387669.1:n.*152A>T
ENST00000473085.1:n.291A>T
ENST00000479674.1:n.677A>T
ENST00000541084.5:c.158A>T	ENSP00000442051.2:p.Glu53Val
NM_000131.4:c.410A>T , LRG_554t1:c.410A>T	NP_000122.1:p.Glu137Val
NM_001267554.1:c.158A>T	NP_001254483.1:p.Glu53Val
NM_019616.3:c.344A>T , LRG_554t2:c.344A>T	NP_062562.1:p.Glu115Val
NR_051961.1:n.431A>T
XM_006719963.2:c.344A>T	XP_006720026.1:p.Glu115Val
XM_011537474.1:c.344A>T	XP_011535776.1:p.Glu115Val
XM_011537475.1:c.158A>T	XP_011535777.1:p.Glu53Val
XM_011537477.1:c.305A>T	XP_011535779.1:p.Glu102Val
XM_006719963.3:c.389A>T	XP_006720026.2:p.Glu130Val
XM_011537474.2:c.389A>T	XP_011535776.2:p.Glu130Val
XM_011537475.2:c.203A>T	XP_011535777.2:p.Glu68Val
NM_019616.4:c.344A>T MANE Select	NP_062562.1:p.Glu115Val
NR_051961.2:n.428A>T
NM_001267554.2:c.158A>T	NP_001254483.1:p.Glu53Val