Canonical Allele Identifier: CA388786017

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772856T>A (hg19) ; chr13:g.113118542T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118542T>A , CM000675.2:g.113118542T>A	GRCh38
NC_000013.10:g.113772856T>A , CM000675.1:g.113772856T>A	GRCh37
NC_000013.9:g.112820857T>A	NCBI36
NG_009258.1:g.744T>A , LRG_548:g.744T>A
NG_009262.1:g.17752T>A , LRG_554:g.17752T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.869T>A MANE Select	ENSP00000329546.4:p.Val290Glu
ENST00000346342.7:c.869T>A	ENSP00000329546.3:p.Val290Glu
ENST00000375581.3:c.935T>A	ENSP00000364731.3:p.Val312Glu
ENST00000541084.5:c.683T>A	ENSP00000442051.2:p.Val228Glu
NM_000131.4:c.935T>A , LRG_554t1:c.935T>A	NP_000122.1:p.Val312Glu
NM_001267554.1:c.683T>A	NP_001254483.1:p.Val228Glu
NM_019616.3:c.869T>A , LRG_554t2:c.869T>A	NP_062562.1:p.Val290Glu
NR_051961.1:n.956T>A
XM_006719963.2:c.728T>A	XP_006720026.1:p.Val243Glu
XM_011537474.1:c.977T>A	XP_011535776.1:p.Val326Glu
XM_011537475.1:c.791T>A	XP_011535777.1:p.Val264Glu
XM_011537476.1:c.629T>A	XP_011535778.1:p.Val210Glu
XM_011537477.1:c.938T>A	XP_011535779.1:p.Val313Glu
XM_006719963.3:c.773T>A	XP_006720026.2:p.Val258Glu
XM_011537474.2:c.1022T>A	XP_011535776.2:p.Val341Glu
XM_011537475.2:c.836T>A	XP_011535777.2:p.Val279Glu
XM_011537476.2:c.629T>A	XP_011535778.1:p.Val210Glu
NM_019616.4:c.869T>A MANE Select	NP_062562.1:p.Val290Glu
NR_051961.2:n.953T>A
NM_001267554.2:c.683T>A	NP_001254483.1:p.Val228Glu