Canonical Allele Identifier: CA1071927817

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1741319191
• gnomAD v3: 4-186287790-CG-C
• gnomAD v4: 4-186287790-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287792del , CM000666.2:g.186287792del	GRCh38
NC_000004.11:g.187208946del , CM000666.1:g.187208946del	GRCh37
NC_000004.10:g.187445940del	NCBI36
NG_008051.1:g.26829del , LRG_583:g.26829del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1685del (F11) MANE Select	ENSP00000384957.2:p.Gly562AlafsTer29
ENST00000264691.4:c.285del (F11)
ENST00000264692.8:c.1523del (F11)	ENSP00000264692.5:p.Gly508AlafsTer29
ENST00000403665.6:c.1685del (F11)	ENSP00000384957.2:p.Gly562AlafsTer29
ENST00000503841.1:n.204del (F11)
NM_000128.3:c.1685del , LRG_583t1:c.1685del (F11)	NP_000119.1:p.Gly562AlafsTer29
NR_033900.1:n.1066+637del (F11-AS1)
XM_005262821.2:c.1688del (F11)	XP_005262878.1:p.Gly563AlafsTer29
XM_005262822.2:c.1592del (F11)	XP_005262879.1:p.Gly531AlafsTer29
XM_005262823.2:c.1418del (F11)	XP_005262880.1:p.Gly473AlafsTer29
XM_006714137.1:c.1640del (F11)	XP_006714200.1:p.Gly547AlafsTer29
XM_005262821.4:c.1688del (F11)	XP_005262878.1:p.Gly563AlafsTer29
XM_005262822.4:c.1592del (F11)	XP_005262879.1:p.Gly531AlafsTer29
XM_005262823.4:c.1418del (F11)	XP_005262880.1:p.Gly473AlafsTer29
XM_006714137.3:c.1640del (F11)	XP_006714200.1:p.Gly547AlafsTer29
NM_000128.4:c.1685del (F11) MANE Select	NP_000119.1:p.Gly562AlafsTer29