Canonical Allele Identifier: CA2623809770

Gene: F7

Linked Data

• gnomAD v4: 13-113119150-A-ACATGTACTCCGTGATATTTGGGGAGTCTCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119150_113119151insCATGTACTCCGTGATATTTGGGGAGTCTCCC , CM000675.2:g.113119150_113119151insCATGTACTCCGTGATATTTGGGGAGTCTCCC	GRCh38
NC_000013.10:g.113773464_113773465insCATGTACTCCGTGATATTTGGGGAGTCTCCC , CM000675.1:g.113773464_113773465insCATGTACTCCGTGATATTTGGGGAGTCTCCC	GRCh37
NC_000013.9:g.112821465_112821466insCATGTACTCCGTGATATTTGGGGAGTCTCCC	NCBI36
NG_009258.1:g.1352_1353insCATGTACTCCGTGATATTTGGGGAGTCTCCC , LRG_548:g.1352_1353insCATGTACTCCGTGATATTTGGGGAGTCTCCC
NG_009262.1:g.18360_18361insCATGTACTCCGTGATATTTGGGGAGTCTCCC , LRG_554:g.18360_18361insCATGTACTCCGTGATATTTGGGGAGTCTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC MANE Select	ENSP00000329546.4:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTC...
ENST00000346342.7:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	ENSP00000329546.3:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTC...
ENST00000375581.3:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	ENSP00000364731.3:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTC...
ENST00000541084.5:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	ENSP00000442051.2:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTC...
NM_000131.4:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC , LRG_554t1:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	NP_000122.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
NM_001267554.1:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	NP_001254483.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
NM_019616.3:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC , LRG_554t2:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	NP_062562.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
NR_051961.1:n.1564_1565insCATGTACTCCGTGATATTTGGGGAGTCTCCC
XM_006719963.2:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	XP_006720026.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
XM_011537474.1:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	XP_011535776.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
XM_011537475.1:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	XP_011535777.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
XM_011537476.1:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	XP_011535778.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
XM_011537477.1:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	XP_011535779.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
XM_006719963.3:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	XP_006720026.2:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
XM_011537474.2:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	XP_011535776.2:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
XM_011537475.2:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	XP_011535777.2:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
XM_011537476.2:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	XP_011535778.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
NM_019616.4:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC MANE Select	NP_062562.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC
NR_051961.2:n.1561_1562insCATGTACTCCGTGATATTTGGGGAGTCTCCC
NM_001267554.2:c.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC	NP_001254483.1:n.*142_*143insCATGTACTCCGTGATATTTGGGGAGTCTCCC