Canonical Allele Identifier: CA13892495

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113116562G>A , CM000675.2:g.113116562G>A	GRCh38
NC_000013.10:g.113770876G>A , CM000675.1:g.113770876G>A	GRCh37
NC_000013.9:g.112818877G>A	NCBI36
NG_009262.1:g.15772G>A , LRG_554:g.15772G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.506-204G>A MANE Select	ENSP00000329546.4:n.506-204G>A
ENST00000346342.7:c.506-204G>A	ENSP00000329546.3:n.506-204G>A
ENST00000375581.3:c.572-204G>A	ENSP00000364731.3:n.572-204G>A
ENST00000444337.1:c.*314-204G>A	ENSP00000387669.1:n.*314-204G>A
ENST00000479674.1:n.698-204G>A
ENST00000541084.5:c.320-204G>A	ENSP00000442051.2:n.320-204G>A
NM_000131.4:c.572-204G>A , LRG_554t1:c.572-204G>A	NP_000122.1:n.572-204G>A
NM_001267554.1:c.320-204G>A	NP_001254483.1:n.320-204G>A
NM_019616.3:c.506-204G>A , LRG_554t2:c.506-204G>A	NP_062562.1:n.506-204G>A
NR_051961.1:n.593-204G>A
XM_006719963.2:c.365-204G>A	XP_006720026.1:n.365-204G>A
XM_011537474.1:c.614-204G>A	XP_011535776.1:n.614-204G>A
XM_011537475.1:c.428-204G>A	XP_011535777.1:n.428-204G>A
XM_011537476.1:c.266-204G>A	XP_011535778.1:n.266-204G>A
XM_011537477.1:c.575-204G>A	XP_011535779.1:n.575-204G>A
XM_006719963.3:c.410-204G>A	XP_006720026.2:n.410-204G>A
XM_011537474.2:c.659-204G>A	XP_011535776.2:n.659-204G>A
XM_011537475.2:c.473-204G>A	XP_011535777.2:n.473-204G>A
XM_011537476.2:c.266-204G>A	XP_011535778.1:n.266-204G>A
NM_019616.4:c.506-204G>A MANE Select	NP_062562.1:n.506-204G>A
NR_051961.2:n.590-204G>A
NM_001267554.2:c.320-204G>A	NP_001254483.1:n.320-204G>A