Canonical Allele Identifier: CA2623810684

Gene: F7

Linked Data

• gnomAD v4: 13-113119533-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119533_113119534insT , CM000675.2:g.113119533_113119534insT	GRCh38
NC_000013.10:g.113773847_113773848insT , CM000675.1:g.113773847_113773848insT	GRCh37
NC_000013.9:g.112821848_112821849insT	NCBI36
NG_009258.1:g.1735_1736insT , LRG_548:g.1735_1736insT
NG_009262.1:g.18743_18744insT , LRG_554:g.18743_18744insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*525_*526insT MANE Select	ENSP00000329546.4:n.*525_*526insT
ENST00000346342.7:c.*525_*526insT	ENSP00000329546.3:n.*525_*526insT
ENST00000375581.3:c.*525_*526insT	ENSP00000364731.3:n.*525_*526insT
ENST00000541084.5:c.*525_*526insT	ENSP00000442051.2:n.*525_*526insT
NM_000131.4:c.*525_*526insT , LRG_554t1:c.*525_*526insT	NP_000122.1:n.*525_*526insT
NM_001267554.1:c.*525_*526insT	NP_001254483.1:n.*525_*526insT
NM_019616.3:c.*525_*526insT , LRG_554t2:c.*525_*526insT	NP_062562.1:n.*525_*526insT
NR_051961.1:n.1947_1948insT
XM_006719963.2:c.*525_*526insT	XP_006720026.1:n.*525_*526insT
XM_011537474.1:c.*525_*526insT	XP_011535776.1:n.*525_*526insT
XM_011537475.1:c.*525_*526insT	XP_011535777.1:n.*525_*526insT
XM_011537476.1:c.*525_*526insT	XP_011535778.1:n.*525_*526insT
XM_011537477.1:c.*525_*526insT	XP_011535779.1:n.*525_*526insT
XM_006719963.3:c.*525_*526insT	XP_006720026.2:n.*525_*526insT
XM_011537474.2:c.*525_*526insT	XP_011535776.2:n.*525_*526insT
XM_011537475.2:c.*525_*526insT	XP_011535777.2:n.*525_*526insT
XM_011537476.2:c.*525_*526insT	XP_011535778.1:n.*525_*526insT
NM_019616.4:c.*525_*526insT MANE Select	NP_062562.1:n.*525_*526insT
NR_051961.2:n.1944_1945insT
NM_001267554.2:c.*525_*526insT	NP_001254483.1:n.*525_*526insT