Canonical Allele Identifier: CA2120143744

Gene: F7

Linked Data

• dbSNP Id: rs2036260225

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119385_113119395del , CM000675.2:g.113119385_113119395del	GRCh38
NC_000013.10:g.113773699_113773709del , CM000675.1:g.113773699_113773709del	GRCh37
NC_000013.9:g.112821700_112821710del	NCBI36
NG_009258.1:g.1587_1597del , LRG_548:g.1587_1597del
NG_009262.1:g.18595_18605del , LRG_554:g.18595_18605del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*377_*387del MANE Select	ENSP00000329546.4:n.*377_*387del
ENST00000346342.7:c.*377_*387del	ENSP00000329546.3:n.*377_*387del
ENST00000375581.3:c.*377_*387del	ENSP00000364731.3:n.*377_*387del
ENST00000541084.5:c.*377_*387del	ENSP00000442051.2:n.*377_*387del
NM_000131.4:c.*377_*387del , LRG_554t1:c.*377_*387del	NP_000122.1:n.*377_*387del
NM_001267554.1:c.*377_*387del	NP_001254483.1:n.*377_*387del
NM_019616.3:c.*377_*387del , LRG_554t2:c.*377_*387del	NP_062562.1:n.*377_*387del
NR_051961.1:n.1799_1809del
XM_006719963.2:c.*377_*387del	XP_006720026.1:n.*377_*387del
XM_011537474.1:c.*377_*387del	XP_011535776.1:n.*377_*387del
XM_011537475.1:c.*377_*387del	XP_011535777.1:n.*377_*387del
XM_011537476.1:c.*377_*387del	XP_011535778.1:n.*377_*387del
XM_011537477.1:c.*377_*387del	XP_011535779.1:n.*377_*387del
XM_006719963.3:c.*377_*387del	XP_006720026.2:n.*377_*387del
XM_011537474.2:c.*377_*387del	XP_011535776.2:n.*377_*387del
XM_011537475.2:c.*377_*387del	XP_011535777.2:n.*377_*387del
XM_011537476.2:c.*377_*387del	XP_011535778.1:n.*377_*387del
NM_019616.4:c.*377_*387del MANE Select	NP_062562.1:n.*377_*387del
NR_051961.2:n.1796_1806del
NM_001267554.2:c.*377_*387del	NP_001254483.1:n.*377_*387del