Canonical Allele Identifier: CA2623808955

Gene: F7

Linked Data

• gnomAD v4: 13-113118532-CACCAGCCCGTGGTCCTCACTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118537_113118557del , CM000675.2:g.113118537_113118557del	GRCh38
NC_000013.10:g.113772851_113772871del , CM000675.1:g.113772851_113772871del	GRCh37
NC_000013.9:g.112820852_112820872del	NCBI36
NG_009258.1:g.739_759del , LRG_548:g.739_759del
NG_009262.1:g.17747_17767del , LRG_554:g.17747_17767del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.864_884del MANE Select	ENSP00000329546.4:p.Gln288_Asp294del
ENST00000346342.7:c.864_884del	ENSP00000329546.3:p.Gln288_Asp294del
ENST00000375581.3:c.930_950del	ENSP00000364731.3:p.Gln310_Asp316del
ENST00000541084.5:c.678_698del	ENSP00000442051.2:p.Gln226_Asp232del
NM_000131.4:c.930_950del , LRG_554t1:c.930_950del	NP_000122.1:p.Gln310_Asp316del
NM_001267554.1:c.678_698del	NP_001254483.1:p.Gln226_Asp232del
NM_019616.3:c.864_884del , LRG_554t2:c.864_884del	NP_062562.1:p.Gln288_Asp294del
NR_051961.1:n.951_971del
XM_006719963.2:c.723_743del	XP_006720026.1:p.Gln241_Asp247del
XM_011537474.1:c.972_992del	XP_011535776.1:p.Gln324_Asp330del
XM_011537475.1:c.786_806del	XP_011535777.1:p.Gln262_Asp268del
XM_011537476.1:c.624_644del	XP_011535778.1:p.Gln208_Asp214del
XM_011537477.1:c.933_953del	XP_011535779.1:p.Gln311_Asp317del
XM_006719963.3:c.768_788del	XP_006720026.2:p.Gln256_Asp262del
XM_011537474.2:c.1017_1037del	XP_011535776.2:p.Gln339_Asp345del
XM_011537475.2:c.831_851del	XP_011535777.2:p.Gln277_Asp283del
XM_011537476.2:c.624_644del	XP_011535778.1:p.Gln208_Asp214del
NM_019616.4:c.864_884del MANE Select	NP_062562.1:p.Gln288_Asp294del
NR_051961.2:n.948_968del
NM_001267554.2:c.678_698del	NP_001254483.1:p.Gln226_Asp232del