Canonical Allele Identifier: CA2729207748

Gene: F7

Linked Data

• dbSNP Id: rs2142235280

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119098_113119099del , CM000675.2:g.113119098_113119099del	GRCh38
NC_000013.10:g.113773412_113773413del , CM000675.1:g.113773412_113773413del	GRCh37
NC_000013.9:g.112821413_112821414del	NCBI36
NG_009258.1:g.1300_1301del , LRG_548:g.1300_1301del
NG_009262.1:g.18308_18309del , LRG_554:g.18308_18309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*90_*91del MANE Select	ENSP00000329546.4:n.*90_*91del
ENST00000346342.7:c.*90_*91del	ENSP00000329546.3:n.*90_*91del
ENST00000375581.3:c.*90_*91del	ENSP00000364731.3:n.*90_*91del
ENST00000541084.5:c.*90_*91del	ENSP00000442051.2:n.*90_*91del
NM_000131.4:c.*90_*91del , LRG_554t1:c.*90_*91del	NP_000122.1:n.*90_*91del
NM_001267554.1:c.*90_*91del	NP_001254483.1:n.*90_*91del
NM_019616.3:c.*90_*91del , LRG_554t2:c.*90_*91del	NP_062562.1:n.*90_*91del
NR_051961.1:n.1512_1513del
XM_006719963.2:c.*90_*91del	XP_006720026.1:n.*90_*91del
XM_011537474.1:c.*90_*91del	XP_011535776.1:n.*90_*91del
XM_011537475.1:c.*90_*91del	XP_011535777.1:n.*90_*91del
XM_011537476.1:c.*90_*91del	XP_011535778.1:n.*90_*91del
XM_011537477.1:c.*90_*91del	XP_011535779.1:n.*90_*91del
XM_006719963.3:c.*90_*91del	XP_006720026.2:n.*90_*91del
XM_011537474.2:c.*90_*91del	XP_011535776.2:n.*90_*91del
XM_011537475.2:c.*90_*91del	XP_011535777.2:n.*90_*91del
XM_011537476.2:c.*90_*91del	XP_011535778.1:n.*90_*91del
NM_019616.4:c.*90_*91del MANE Select	NP_062562.1:n.*90_*91del
NR_051961.2:n.1509_1510del
NM_001267554.2:c.*90_*91del	NP_001254483.1:n.*90_*91del