Canonical Allele Identifier: CA2800664066

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118987_113118989del , CM000675.2:g.113118987_113118989del	GRCh38
NC_000013.10:g.113773301_113773303del , CM000675.1:g.113773301_113773303del	GRCh37
NC_000013.9:g.112821302_112821304del	NCBI36
NG_009258.1:g.1189_1191del , LRG_548:g.1189_1191del
NG_009262.1:g.18197_18199del , LRG_554:g.18197_18199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1314_1316del MANE Select	ENSP00000329546.4:p.Leu439del
ENST00000346342.7:c.1314_1316del	ENSP00000329546.3:p.Leu439del
ENST00000375581.3:c.1380_1382del	ENSP00000364731.3:p.Leu461del
ENST00000541084.5:c.1128_1130del	ENSP00000442051.2:p.Leu377del
NM_000131.4:c.1380_1382del , LRG_554t1:c.1380_1382del	NP_000122.1:p.Leu461del
NM_001267554.1:c.1128_1130del	NP_001254483.1:p.Leu377del
NM_019616.3:c.1314_1316del , LRG_554t2:c.1314_1316del	NP_062562.1:p.Leu439del
NR_051961.1:n.1401_1403del
XM_006719963.2:c.1173_1175del	XP_006720026.1:p.Leu392del
XM_011537474.1:c.1422_1424del	XP_011535776.1:p.Leu475del
XM_011537475.1:c.1236_1238del	XP_011535777.1:p.Leu413del
XM_011537476.1:c.1074_1076del	XP_011535778.1:p.Leu359del
XM_011537477.1:c.1383_1385del	XP_011535779.1:p.Leu462del
XM_006719963.3:c.1218_1220del	XP_006720026.2:p.Leu407del
XM_011537474.2:c.1467_1469del	XP_011535776.2:p.Leu490del
XM_011537475.2:c.1281_1283del	XP_011535777.2:p.Leu428del
XM_011537476.2:c.1074_1076del	XP_011535778.1:p.Leu359del
NM_019616.4:c.1314_1316del MANE Select	NP_062562.1:p.Leu439del
NR_051961.2:n.1398_1400del
NM_001267554.2:c.1128_1130del	NP_001254483.1:p.Leu377del