Canonical Allele Identifier: CA2120144050

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119530_113119532delinsCAG , CM000675.2:g.113119530_113119532delinsCAG	GRCh38
NC_000013.10:g.113773844_113773846delinsCAG , CM000675.1:g.113773844_113773846delinsCAG	GRCh37
NC_000013.9:g.112821845_112821847delinsCAG	NCBI36
NG_009258.1:g.1732_1734delinsCAG , LRG_548:g.1732_1734delinsCAG
NG_009262.1:g.18740_18742delinsCAG , LRG_554:g.18740_18742delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*522_*524delinsCAG MANE Select	ENSP00000329546.4:n.*522_*524delinsCAG
ENST00000346342.7:c.*522_*524delinsCAG	ENSP00000329546.3:n.*522_*524delinsCAG
ENST00000375581.3:c.*522_*524delinsCAG	ENSP00000364731.3:n.*522_*524delinsCAG
ENST00000541084.5:c.*522_*524delinsCAG	ENSP00000442051.2:n.*522_*524delinsCAG
NM_000131.4:c.*522_*524delinsCAG , LRG_554t1:c.*522_*524delinsCAG	NP_000122.1:n.*522_*524delinsCAG
NM_001267554.1:c.*522_*524delinsCAG	NP_001254483.1:n.*522_*524delinsCAG
NM_019616.3:c.*522_*524delinsCAG , LRG_554t2:c.*522_*524delinsCAG	NP_062562.1:n.*522_*524delinsCAG
NR_051961.1:n.1944_1946delinsCAG
XM_006719963.2:c.*522_*524delinsCAG	XP_006720026.1:n.*522_*524delinsCAG
XM_011537474.1:c.*522_*524delinsCAG	XP_011535776.1:n.*522_*524delinsCAG
XM_011537475.1:c.*522_*524delinsCAG	XP_011535777.1:n.*522_*524delinsCAG
XM_011537476.1:c.*522_*524delinsCAG	XP_011535778.1:n.*522_*524delinsCAG
XM_011537477.1:c.*522_*524delinsCAG	XP_011535779.1:n.*522_*524delinsCAG
XM_006719963.3:c.*522_*524delinsCAG	XP_006720026.2:n.*522_*524delinsCAG
XM_011537474.2:c.*522_*524delinsCAG	XP_011535776.2:n.*522_*524delinsCAG
XM_011537475.2:c.*522_*524delinsCAG	XP_011535777.2:n.*522_*524delinsCAG
XM_011537476.2:c.*522_*524delinsCAG	XP_011535778.1:n.*522_*524delinsCAG
NM_019616.4:c.*522_*524delinsCAG MANE Select	NP_062562.1:n.*522_*524delinsCAG
NR_051961.2:n.1941_1943delinsCAG
NM_001267554.2:c.*522_*524delinsCAG	NP_001254483.1:n.*522_*524delinsCAG