Canonical Allele Identifier: CA2120143394

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119115_113119129delinsAGGGAGGGAGAGGTG , CM000675.2:g.113119115_113119129delinsAGGGAGGGAGAGGTG	GRCh38
NC_000013.10:g.113773429_113773443delinsAGGGAGGGAGAGGTG , CM000675.1:g.113773429_113773443delinsAGGGAGGGAGAGGTG	GRCh37
NC_000013.9:g.112821430_112821444delinsAGGGAGGGAGAGGTG	NCBI36
NG_009258.1:g.1317_1331delinsAGGGAGGGAGAGGTG , LRG_548:g.1317_1331delinsAGGGAGGGAGAGGTG
NG_009262.1:g.18325_18339delinsAGGGAGGGAGAGGTG , LRG_554:g.18325_18339delinsAGGGAGGGAGAGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*107_*121delinsAGGGAGGGAGAGGTG MANE Select	ENSP00000329546.4:n.*107_*121delinsAGGGAGGGAGAGGTG
ENST00000346342.7:c.*107_*121delinsAGGGAGGGAGAGGTG	ENSP00000329546.3:n.*107_*121delinsAGGGAGGGAGAGGTG
ENST00000375581.3:c.*107_*121delinsAGGGAGGGAGAGGTG	ENSP00000364731.3:n.*107_*121delinsAGGGAGGGAGAGGTG
ENST00000541084.5:c.*107_*121delinsAGGGAGGGAGAGGTG	ENSP00000442051.2:n.*107_*121delinsAGGGAGGGAGAGGTG
NM_000131.4:c.*107_*121delinsAGGGAGGGAGAGGTG , LRG_554t1:c.*107_*121delinsAGGGAGGGAGAGGTG	NP_000122.1:n.*107_*121delinsAGGGAGGGAGAGGTG
NM_001267554.1:c.*107_*121delinsAGGGAGGGAGAGGTG	NP_001254483.1:n.*107_*121delinsAGGGAGGGAGAGGTG
NM_019616.3:c.*107_*121delinsAGGGAGGGAGAGGTG , LRG_554t2:c.*107_*121delinsAGGGAGGGAGAGGTG	NP_062562.1:n.*107_*121delinsAGGGAGGGAGAGGTG
NR_051961.1:n.1529_1543delinsAGGGAGGGAGAGGTG
XM_006719963.2:c.*107_*121delinsAGGGAGGGAGAGGTG	XP_006720026.1:n.*107_*121delinsAGGGAGGGAGAGGTG
XM_011537474.1:c.*107_*121delinsAGGGAGGGAGAGGTG	XP_011535776.1:n.*107_*121delinsAGGGAGGGAGAGGTG
XM_011537475.1:c.*107_*121delinsAGGGAGGGAGAGGTG	XP_011535777.1:n.*107_*121delinsAGGGAGGGAGAGGTG
XM_011537476.1:c.*107_*121delinsAGGGAGGGAGAGGTG	XP_011535778.1:n.*107_*121delinsAGGGAGGGAGAGGTG
XM_011537477.1:c.*107_*121delinsAGGGAGGGAGAGGTG	XP_011535779.1:n.*107_*121delinsAGGGAGGGAGAGGTG
XM_006719963.3:c.*107_*121delinsAGGGAGGGAGAGGTG	XP_006720026.2:n.*107_*121delinsAGGGAGGGAGAGGTG
XM_011537474.2:c.*107_*121delinsAGGGAGGGAGAGGTG	XP_011535776.2:n.*107_*121delinsAGGGAGGGAGAGGTG
XM_011537475.2:c.*107_*121delinsAGGGAGGGAGAGGTG	XP_011535777.2:n.*107_*121delinsAGGGAGGGAGAGGTG
XM_011537476.2:c.*107_*121delinsAGGGAGGGAGAGGTG	XP_011535778.1:n.*107_*121delinsAGGGAGGGAGAGGTG
NM_019616.4:c.*107_*121delinsAGGGAGGGAGAGGTG MANE Select	NP_062562.1:n.*107_*121delinsAGGGAGGGAGAGGTG
NR_051961.2:n.1526_1540delinsAGGGAGGGAGAGGTG
NM_001267554.2:c.*107_*121delinsAGGGAGGGAGAGGTG	NP_001254483.1:n.*107_*121delinsAGGGAGGGAGAGGTG