Canonical Allele Identifier: CA2120144824

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119854_113119855delinsCT , CM000675.2:g.113119854_113119855delinsCT	GRCh38
NC_000013.10:g.113774168_113774169delinsCT , CM000675.1:g.113774168_113774169delinsCT	GRCh37
NC_000013.9:g.112822169_112822170delinsCT	NCBI36
NG_009258.1:g.2056_2057delinsCT , LRG_548:g.2056_2057delinsCT
NG_009262.1:g.19064_19065delinsCT , LRG_554:g.19064_19065delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*846_*847delinsCT MANE Select	ENSP00000329546.4:n.*846_*847delinsCT
ENST00000346342.7:c.*846_*847delinsCT	ENSP00000329546.3:n.*846_*847delinsCT
ENST00000375581.3:c.*846_*847delinsCT	ENSP00000364731.3:n.*846_*847delinsCT
ENST00000541084.5:c.*846_*847delinsCT	ENSP00000442051.2:n.*846_*847delinsCT
NM_000131.4:c.*846_*847delinsCT , LRG_554t1:c.*846_*847delinsCT	NP_000122.1:n.*846_*847delinsCT
NM_001267554.1:c.*846_*847delinsCT	NP_001254483.1:n.*846_*847delinsCT
NM_019616.3:c.*846_*847delinsCT , LRG_554t2:c.*846_*847delinsCT	NP_062562.1:n.*846_*847delinsCT
NR_051961.1:n.2268_2269delinsCT
XM_006719963.2:c.*846_*847delinsCT	XP_006720026.1:n.*846_*847delinsCT
XM_011537474.1:c.*846_*847delinsCT	XP_011535776.1:n.*846_*847delinsCT
XM_011537475.1:c.*846_*847delinsCT	XP_011535777.1:n.*846_*847delinsCT
XM_011537476.1:c.*846_*847delinsCT	XP_011535778.1:n.*846_*847delinsCT
XM_011537477.1:c.*846_*847delinsCT	XP_011535779.1:n.*846_*847delinsCT
XM_006719963.3:c.*846_*847delinsCT	XP_006720026.2:n.*846_*847delinsCT
XM_011537474.2:c.*846_*847delinsCT	XP_011535776.2:n.*846_*847delinsCT
XM_011537475.2:c.*846_*847delinsCT	XP_011535777.2:n.*846_*847delinsCT
XM_011537476.2:c.*846_*847delinsCT	XP_011535778.1:n.*846_*847delinsCT
NM_019616.4:c.*846_*847delinsCT MANE Select	NP_062562.1:n.*846_*847delinsCT
NR_051961.2:n.2265_2266delinsCT
NM_001267554.2:c.*846_*847delinsCT	NP_001254483.1:n.*846_*847delinsCT