Canonical Allele Identifier: CA2623809295

Gene: F7

Linked Data

• gnomAD v4: 13-113118829-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118830_113118831del , CM000675.2:g.113118830_113118831del	GRCh38
NC_000013.10:g.113773144_113773145del , CM000675.1:g.113773144_113773145del	GRCh37
NC_000013.9:g.112821145_112821146del	NCBI36
NG_009258.1:g.1032_1033del , LRG_548:g.1032_1033del
NG_009262.1:g.18040_18041del , LRG_554:g.18040_18041del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1157_1158del MANE Select	ENSP00000329546.4:p.His386ArgfsTer?
ENST00000346342.7:c.1157_1158del	ENSP00000329546.3:p.His386ArgfsTer?
ENST00000375581.3:c.1223_1224del	ENSP00000364731.3:p.His408ArgfsTer?
ENST00000541084.5:c.971_972del	ENSP00000442051.2:p.His324ArgfsTer?
NM_000131.4:c.1223_1224del , LRG_554t1:c.1223_1224del	NP_000122.1:p.His408ArgfsTer?
NM_001267554.1:c.971_972del	NP_001254483.1:p.His324ArgfsTer?
NM_019616.3:c.1157_1158del , LRG_554t2:c.1157_1158del	NP_062562.1:p.His386ArgfsTer?
NR_051961.1:n.1244_1245del
XM_006719963.2:c.1016_1017del	XP_006720026.1:p.His339ArgfsTer?
XM_011537474.1:c.1265_1266del	XP_011535776.1:p.His422ArgfsTer?
XM_011537475.1:c.1079_1080del	XP_011535777.1:p.His360ArgfsTer?
XM_011537476.1:c.917_918del	XP_011535778.1:p.His306ArgfsTer?
XM_011537477.1:c.1226_1227del	XP_011535779.1:p.His409ArgfsTer?
XM_006719963.3:c.1061_1062del	XP_006720026.2:p.His354ArgfsTer?
XM_011537474.2:c.1310_1311del	XP_011535776.2:p.His437ArgfsTer?
XM_011537475.2:c.1124_1125del	XP_011535777.2:p.His375ArgfsTer?
XM_011537476.2:c.917_918del	XP_011535778.1:p.His306ArgfsTer?
NM_019616.4:c.1157_1158del MANE Select	NP_062562.1:p.His386ArgfsTer?
NR_051961.2:n.1241_1242del
NM_001267554.2:c.971_972del	NP_001254483.1:p.His324ArgfsTer?