Canonical Allele Identifier: CA2120143539

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119213_113119215delinsCAA , CM000675.2:g.113119213_113119215delinsCAA	GRCh38
NC_000013.10:g.113773527_113773529delinsCAA , CM000675.1:g.113773527_113773529delinsCAA	GRCh37
NC_000013.9:g.112821528_112821530delinsCAA	NCBI36
NG_009258.1:g.1415_1417delinsCAA , LRG_548:g.1415_1417delinsCAA
NG_009262.1:g.18423_18425delinsCAA , LRG_554:g.18423_18425delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*205_*207delinsCAA MANE Select	ENSP00000329546.4:n.*205_*207delinsCAA
ENST00000346342.7:c.*205_*207delinsCAA	ENSP00000329546.3:n.*205_*207delinsCAA
ENST00000375581.3:c.*205_*207delinsCAA	ENSP00000364731.3:n.*205_*207delinsCAA
ENST00000541084.5:c.*205_*207delinsCAA	ENSP00000442051.2:n.*205_*207delinsCAA
NM_000131.4:c.*205_*207delinsCAA , LRG_554t1:c.*205_*207delinsCAA	NP_000122.1:n.*205_*207delinsCAA
NM_001267554.1:c.*205_*207delinsCAA	NP_001254483.1:n.*205_*207delinsCAA
NM_019616.3:c.*205_*207delinsCAA , LRG_554t2:c.*205_*207delinsCAA	NP_062562.1:n.*205_*207delinsCAA
NR_051961.1:n.1627_1629delinsCAA
XM_006719963.2:c.*205_*207delinsCAA	XP_006720026.1:n.*205_*207delinsCAA
XM_011537474.1:c.*205_*207delinsCAA	XP_011535776.1:n.*205_*207delinsCAA
XM_011537475.1:c.*205_*207delinsCAA	XP_011535777.1:n.*205_*207delinsCAA
XM_011537476.1:c.*205_*207delinsCAA	XP_011535778.1:n.*205_*207delinsCAA
XM_011537477.1:c.*205_*207delinsCAA	XP_011535779.1:n.*205_*207delinsCAA
XM_006719963.3:c.*205_*207delinsCAA	XP_006720026.2:n.*205_*207delinsCAA
XM_011537474.2:c.*205_*207delinsCAA	XP_011535776.2:n.*205_*207delinsCAA
XM_011537475.2:c.*205_*207delinsCAA	XP_011535777.2:n.*205_*207delinsCAA
XM_011537476.2:c.*205_*207delinsCAA	XP_011535778.1:n.*205_*207delinsCAA
NM_019616.4:c.*205_*207delinsCAA MANE Select	NP_062562.1:n.*205_*207delinsCAA
NR_051961.2:n.1624_1626delinsCAA
NM_001267554.2:c.*205_*207delinsCAA	NP_001254483.1:n.*205_*207delinsCAA