Canonical Allele Identifier: CA2623810442

Gene: F7

Linked Data

• gnomAD v4: 13-113119472-CGCCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119473_113119476del , CM000675.2:g.113119473_113119476del	GRCh38
NC_000013.10:g.113773787_113773790del , CM000675.1:g.113773787_113773790del	GRCh37
NC_000013.9:g.112821788_112821791del	NCBI36
NG_009258.1:g.1675_1678del , LRG_548:g.1675_1678del
NG_009262.1:g.18683_18686del , LRG_554:g.18683_18686del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*465_*468del MANE Select	ENSP00000329546.4:n.*465_*468del
ENST00000346342.7:c.*465_*468del	ENSP00000329546.3:n.*465_*468del
ENST00000375581.3:c.*465_*468del	ENSP00000364731.3:n.*465_*468del
ENST00000541084.5:c.*465_*468del	ENSP00000442051.2:n.*465_*468del
NM_000131.4:c.*465_*468del , LRG_554t1:c.*465_*468del	NP_000122.1:n.*465_*468del
NM_001267554.1:c.*465_*468del	NP_001254483.1:n.*465_*468del
NM_019616.3:c.*465_*468del , LRG_554t2:c.*465_*468del	NP_062562.1:n.*465_*468del
NR_051961.1:n.1887_1890del
XM_006719963.2:c.*465_*468del	XP_006720026.1:n.*465_*468del
XM_011537474.1:c.*465_*468del	XP_011535776.1:n.*465_*468del
XM_011537475.1:c.*465_*468del	XP_011535777.1:n.*465_*468del
XM_011537476.1:c.*465_*468del	XP_011535778.1:n.*465_*468del
XM_011537477.1:c.*465_*468del	XP_011535779.1:n.*465_*468del
XM_006719963.3:c.*465_*468del	XP_006720026.2:n.*465_*468del
XM_011537474.2:c.*465_*468del	XP_011535776.2:n.*465_*468del
XM_011537475.2:c.*465_*468del	XP_011535777.2:n.*465_*468del
XM_011537476.2:c.*465_*468del	XP_011535778.1:n.*465_*468del
NM_019616.4:c.*465_*468del MANE Select	NP_062562.1:n.*465_*468del
NR_051961.2:n.1884_1887del
NM_001267554.2:c.*465_*468del	NP_001254483.1:n.*465_*468del