Canonical Allele Identifier: CA2800652010

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118307G>A , CM000675.2:g.113118307G>A	GRCh38
NC_000013.10:g.113772621G>A , CM000675.1:g.113772621G>A	GRCh37
NC_000013.9:g.112820622G>A	NCBI36
NG_009258.1:g.509G>A , LRG_548:g.509G>A
NG_009262.1:g.17517G>A , LRG_554:g.17517G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.740-106G>A MANE Select	ENSP00000329546.4:n.740-106G>A
ENST00000346342.7:c.740-106G>A	ENSP00000329546.3:n.740-106G>A
ENST00000375581.3:c.806-106G>A	ENSP00000364731.3:n.806-106G>A
ENST00000541084.5:c.554-106G>A	ENSP00000442051.2:n.554-106G>A
NM_000131.4:c.806-106G>A , LRG_554t1:c.806-106G>A	NP_000122.1:n.806-106G>A
NM_001267554.1:c.554-106G>A	NP_001254483.1:n.554-106G>A
NM_019616.3:c.740-106G>A , LRG_554t2:c.740-106G>A	NP_062562.1:n.740-106G>A
NR_051961.1:n.827-106G>A
XM_006719963.2:c.599-106G>A	XP_006720026.1:n.599-106G>A
XM_011537474.1:c.848-106G>A	XP_011535776.1:n.848-106G>A
XM_011537475.1:c.662-106G>A	XP_011535777.1:n.662-106G>A
XM_011537476.1:c.500-106G>A	XP_011535778.1:n.500-106G>A
XM_011537477.1:c.809-106G>A	XP_011535779.1:n.809-106G>A
XM_006719963.3:c.644-106G>A	XP_006720026.2:n.644-106G>A
XM_011537474.2:c.893-106G>A	XP_011535776.2:n.893-106G>A
XM_011537475.2:c.707-106G>A	XP_011535777.2:n.707-106G>A
XM_011537476.2:c.500-106G>A	XP_011535778.1:n.500-106G>A
NM_019616.4:c.740-106G>A MANE Select	NP_062562.1:n.740-106G>A
NR_051961.2:n.824-106G>A
NM_001267554.2:c.554-106G>A	NP_001254483.1:n.554-106G>A