Canonical Allele Identifier: CA388785975

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772832C>A (hg19) ; chr13:g.113118518C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118518C>A , CM000675.2:g.113118518C>A	GRCh38
NC_000013.10:g.113772832C>A , CM000675.1:g.113772832C>A	GRCh37
NC_000013.9:g.112820833C>A	NCBI36
NG_009258.1:g.720C>A , LRG_548:g.720C>A
NG_009262.1:g.17728C>A , LRG_554:g.17728C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.845C>A MANE Select	ENSP00000329546.4:p.Ala282Glu
ENST00000346342.7:c.845C>A	ENSP00000329546.3:p.Ala282Glu
ENST00000375581.3:c.911C>A	ENSP00000364731.3:p.Ala304Glu
ENST00000541084.5:c.659C>A	ENSP00000442051.2:p.Ala220Glu
NM_000131.4:c.911C>A , LRG_554t1:c.911C>A	NP_000122.1:p.Ala304Glu
NM_001267554.1:c.659C>A	NP_001254483.1:p.Ala220Glu
NM_019616.3:c.845C>A , LRG_554t2:c.845C>A	NP_062562.1:p.Ala282Glu
NR_051961.1:n.932C>A
XM_006719963.2:c.704C>A	XP_006720026.1:p.Ala235Glu
XM_011537474.1:c.953C>A	XP_011535776.1:p.Ala318Glu
XM_011537475.1:c.767C>A	XP_011535777.1:p.Ala256Glu
XM_011537476.1:c.605C>A	XP_011535778.1:p.Ala202Glu
XM_011537477.1:c.914C>A	XP_011535779.1:p.Ala305Glu
XM_006719963.3:c.749C>A	XP_006720026.2:p.Ala250Glu
XM_011537474.2:c.998C>A	XP_011535776.2:p.Ala333Glu
XM_011537475.2:c.812C>A	XP_011535777.2:p.Ala271Glu
XM_011537476.2:c.605C>A	XP_011535778.1:p.Ala202Glu
NM_019616.4:c.845C>A MANE Select	NP_062562.1:p.Ala282Glu
NR_051961.2:n.929C>A
NM_001267554.2:c.659C>A	NP_001254483.1:p.Ala220Glu