Canonical Allele Identifier: CA2120143767

Gene: F7

Linked Data

• dbSNP Id: rs2036260624

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119398_113119399insGCTCAGGCTGCTGCTCTGCCGG , CM000675.2:g.113119398_113119399insGCTCAGGCTGCTGCTCTGCCGG	GRCh38
NC_000013.10:g.113773712_113773713insGCTCAGGCTGCTGCTCTGCCGG , CM000675.1:g.113773712_113773713insGCTCAGGCTGCTGCTCTGCCGG	GRCh37
NC_000013.9:g.112821713_112821714insGCTCAGGCTGCTGCTCTGCCGG	NCBI36
NG_009258.1:g.1600_1601insGCTCAGGCTGCTGCTCTGCCGG , LRG_548:g.1600_1601insGCTCAGGCTGCTGCTCTGCCGG
NG_009262.1:g.18608_18609insGCTCAGGCTGCTGCTCTGCCGG , LRG_554:g.18608_18609insGCTCAGGCTGCTGCTCTGCCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG MANE Select	ENSP00000329546.4:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
ENST00000346342.7:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	ENSP00000329546.3:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
ENST00000375581.3:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	ENSP00000364731.3:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
ENST00000541084.5:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	ENSP00000442051.2:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
NM_000131.4:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG , LRG_554t1:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	NP_000122.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
NM_001267554.1:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	NP_001254483.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
NM_019616.3:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG , LRG_554t2:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	NP_062562.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
NR_051961.1:n.1812_1813insGCTCAGGCTGCTGCTCTGCCGG
XM_006719963.2:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	XP_006720026.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
XM_011537474.1:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	XP_011535776.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
XM_011537475.1:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	XP_011535777.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
XM_011537476.1:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	XP_011535778.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
XM_011537477.1:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	XP_011535779.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
XM_006719963.3:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	XP_006720026.2:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
XM_011537474.2:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	XP_011535776.2:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
XM_011537475.2:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	XP_011535777.2:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
XM_011537476.2:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	XP_011535778.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
NM_019616.4:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG MANE Select	NP_062562.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG
NR_051961.2:n.1809_1810insGCTCAGGCTGCTGCTCTGCCGG
NM_001267554.2:c.*390_*391insGCTCAGGCTGCTGCTCTGCCGG	NP_001254483.1:n.*390_*391insGCTCAGGCTGCTGCTCTGCCGG