Canonical Allele Identifier: CA2575461716

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118335del , CM000675.2:g.113118335del	GRCh38
NC_000013.10:g.113772649del , CM000675.1:g.113772649del	GRCh37
NC_000013.9:g.112820650del	NCBI36
NG_009258.1:g.537del , LRG_548:g.537del
NG_009262.1:g.17545del , LRG_554:g.17545del

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.740-78del MANE Select	ENSP00000329546.4:n.740-78del
ENST00000346342.7:c.740-78del	ENSP00000329546.3:n.740-78del
ENST00000375581.3:c.806-78del	ENSP00000364731.3:n.806-78del
ENST00000541084.5:c.554-78del	ENSP00000442051.2:n.554-78del
NM_000131.4:c.806-78del , LRG_554t1:c.806-78del	NP_000122.1:n.806-78del
NM_001267554.1:c.554-78del	NP_001254483.1:n.554-78del
NM_019616.3:c.740-78del , LRG_554t2:c.740-78del	NP_062562.1:n.740-78del
NR_051961.1:n.827-78del
XM_006719963.2:c.599-78del	XP_006720026.1:n.599-78del
XM_011537474.1:c.848-78del	XP_011535776.1:n.848-78del
XM_011537475.1:c.662-78del	XP_011535777.1:n.662-78del
XM_011537476.1:c.500-78del	XP_011535778.1:n.500-78del
XM_011537477.1:c.809-78del	XP_011535779.1:n.809-78del
XM_006719963.3:c.644-78del	XP_006720026.2:n.644-78del
XM_011537474.2:c.893-78del	XP_011535776.2:n.893-78del
XM_011537475.2:c.707-78del	XP_011535777.2:n.707-78del
XM_011537476.2:c.500-78del	XP_011535778.1:n.500-78del
NM_019616.4:c.740-78del MANE Select	NP_062562.1:n.740-78del
NR_051961.2:n.824-78del
NM_001267554.2:c.554-78del	NP_001254483.1:n.554-78del