Canonical Allele Identifier: CA1519938503

Gene: F11

Linked Data

• dbSNP Id: rs1741151518
• gnomAD v4: 4-186285675-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285679del , CM000666.2:g.186285679del	GRCh38
NC_000004.11:g.187206833del , CM000666.1:g.187206833del	GRCh37
NC_000004.10:g.187443827del	NCBI36
NG_008051.1:g.24716del , LRG_583:g.24716del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1346del MANE Select	ENSP00000384957.2:p.Leu449Ter
ENST00000264691.4:c.42del
ENST00000264692.8:c.1184del	ENSP00000264692.5:p.Leu395Ter
ENST00000403665.6:c.1346del	ENSP00000384957.2:p.Leu449Ter
NM_000128.3:c.1346del , LRG_583t1:c.1346del	NP_000119.1:p.Leu449Ter
XM_005262821.2:c.1349del	XP_005262878.1:p.Leu450Ter
XM_005262822.2:c.1349del	XP_005262879.1:p.Leu450Ter
XM_005262823.2:c.1079del	XP_005262880.1:p.Leu360Ter
XM_005262824.1:c.1349del	XP_005262881.1:p.Leu450Ter
XM_006714137.1:c.1301del	XP_006714200.1:p.Leu434Ter
XR_938706.1:n.1754del
XR_938707.1:n.1754del
XM_005262821.4:c.1349del	XP_005262878.1:p.Leu450Ter
XM_005262822.4:c.1349del	XP_005262879.1:p.Leu450Ter
XM_005262823.4:c.1079del	XP_005262880.1:p.Leu360Ter
XM_006714137.3:c.1301del	XP_006714200.1:p.Leu434Ter
XR_001741172.2:n.1820del
NM_000128.4:c.1346del MANE Select	NP_000119.1:p.Leu449Ter