Canonical Allele Identifier: CA388785862

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772775T>A (hg19) ; chr13:g.113118461T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118461T>A , CM000675.2:g.113118461T>A	GRCh38
NC_000013.10:g.113772775T>A , CM000675.1:g.113772775T>A	GRCh37
NC_000013.9:g.112820776T>A	NCBI36
NG_009258.1:g.663T>A , LRG_548:g.663T>A
NG_009262.1:g.17671T>A , LRG_554:g.17671T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.788T>A MANE Select	ENSP00000329546.4:p.Val263Glu
ENST00000346342.7:c.788T>A	ENSP00000329546.3:p.Val263Glu
ENST00000375581.3:c.854T>A	ENSP00000364731.3:p.Val285Glu
ENST00000541084.5:c.602T>A	ENSP00000442051.2:p.Val201Glu
NM_000131.4:c.854T>A , LRG_554t1:c.854T>A	NP_000122.1:p.Val285Glu
NM_001267554.1:c.602T>A	NP_001254483.1:p.Val201Glu
NM_019616.3:c.788T>A , LRG_554t2:c.788T>A	NP_062562.1:p.Val263Glu
NR_051961.1:n.875T>A
XM_006719963.2:c.647T>A	XP_006720026.1:p.Val216Glu
XM_011537474.1:c.896T>A	XP_011535776.1:p.Val299Glu
XM_011537475.1:c.710T>A	XP_011535777.1:p.Val237Glu
XM_011537476.1:c.548T>A	XP_011535778.1:p.Val183Glu
XM_011537477.1:c.857T>A	XP_011535779.1:p.Val286Glu
XM_006719963.3:c.692T>A	XP_006720026.2:p.Val231Glu
XM_011537474.2:c.941T>A	XP_011535776.2:p.Val314Glu
XM_011537475.2:c.755T>A	XP_011535777.2:p.Val252Glu
XM_011537476.2:c.548T>A	XP_011535778.1:p.Val183Glu
NM_019616.4:c.788T>A MANE Select	NP_062562.1:p.Val263Glu
NR_051961.2:n.872T>A
NM_001267554.2:c.602T>A	NP_001254483.1:p.Val201Glu