Canonical Allele Identifier: CA2120141891

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118469_113118472delinsGTCA , CM000675.2:g.113118469_113118472delinsGTCA	GRCh38
NC_000013.10:g.113772783_113772786delinsGTCA , CM000675.1:g.113772783_113772786delinsGTCA	GRCh37
NC_000013.9:g.112820784_112820787delinsGTCA	NCBI36
NG_009258.1:g.671_674delinsGTCA , LRG_548:g.671_674delinsGTCA
NG_009262.1:g.17679_17682delinsGTCA , LRG_554:g.17679_17682delinsGTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.796_799delinsGTCA MANE Select	ENSP00000329546.4:p.Val266=
ENST00000346342.7:c.796_799delinsGTCA	ENSP00000329546.3:p.Val266=
ENST00000375581.3:c.862_865delinsGTCA	ENSP00000364731.3:p.Val288=
ENST00000541084.5:c.610_613delinsGTCA	ENSP00000442051.2:p.Val204=
NM_000131.4:c.862_865delinsGTCA , LRG_554t1:c.862_865delinsGTCA	NP_000122.1:p.Val288=
NM_001267554.1:c.610_613delinsGTCA	NP_001254483.1:p.Val204=
NM_019616.3:c.796_799delinsGTCA , LRG_554t2:c.796_799delinsGTCA	NP_062562.1:p.Val266=
NR_051961.1:n.883_886delinsGTCA
XM_006719963.2:c.655_658delinsGTCA	XP_006720026.1:p.Val219=
XM_011537474.1:c.904_907delinsGTCA	XP_011535776.1:p.Val302=
XM_011537475.1:c.718_721delinsGTCA	XP_011535777.1:p.Val240=
XM_011537476.1:c.556_559delinsGTCA	XP_011535778.1:p.Val186=
XM_011537477.1:c.865_868delinsGTCA	XP_011535779.1:p.Val289=
XM_006719963.3:c.700_703delinsGTCA	XP_006720026.2:p.Val234=
XM_011537474.2:c.949_952delinsGTCA	XP_011535776.2:p.Val317=
XM_011537475.2:c.763_766delinsGTCA	XP_011535777.2:p.Val255=
XM_011537476.2:c.556_559delinsGTCA	XP_011535778.1:p.Val186=
NM_019616.4:c.796_799delinsGTCA MANE Select	NP_062562.1:p.Val266=
NR_051961.2:n.880_883delinsGTCA
NM_001267554.2:c.610_613delinsGTCA	NP_001254483.1:p.Val204=