Canonical Allele Identifier: CA1071927889

Gene: F11 F11-AS1

Linked Data

• gnomAD v3: 4-186288086-T-TG
• gnomAD v4: 4-186288086-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288086_186288087insG , CM000666.2:g.186288086_186288087insG	GRCh38
NC_000004.11:g.187209240_187209241insG , CM000666.1:g.187209240_187209241insG	GRCh37
NC_000004.10:g.187446234_187446235insG	NCBI36
NG_008051.1:g.27123_27124insG , LRG_583:g.27123_27124insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+263_1716+264insG (F11) MANE Select	ENSP00000384957.2:n.1716+263_1716+264insG
ENST00000264691.4:c.316+263_316+264insG (F11)
ENST00000264692.8:c.1554+263_1554+264insG (F11)	ENSP00000264692.5:n.1554+263_1554+264insG
ENST00000403665.6:c.1716+263_1716+264insG (F11)	ENSP00000384957.2:n.1716+263_1716+264insG
ENST00000503841.1:n.235+263_235+264insG (F11)
NM_000128.3:c.1716+263_1716+264insG , LRG_583t1:c.1716+263_1716+264insG (F11)	NP_000119.1:n.1716+263_1716+264insG
NR_033900.1:n.1066+341_1066+342insC (F11-AS1)
XM_005262821.2:c.1719+263_1719+264insG (F11)	XP_005262878.1:n.1719+263_1719+264insG
XM_005262822.2:c.1623+263_1623+264insG (F11)	XP_005262879.1:n.1623+263_1623+264insG
XM_005262823.2:c.1449+263_1449+264insG (F11)	XP_005262880.1:n.1449+263_1449+264insG
XM_006714137.1:c.1671+263_1671+264insG (F11)	XP_006714200.1:n.1671+263_1671+264insG
XM_005262821.4:c.1719+263_1719+264insG (F11)	XP_005262878.1:n.1719+263_1719+264insG
XM_005262822.4:c.1623+263_1623+264insG (F11)	XP_005262879.1:n.1623+263_1623+264insG
XM_005262823.4:c.1449+263_1449+264insG (F11)	XP_005262880.1:n.1449+263_1449+264insG
XM_006714137.3:c.1671+263_1671+264insG (F11)	XP_006714200.1:n.1671+263_1671+264insG
NM_000128.4:c.1716+263_1716+264insG (F11) MANE Select	NP_000119.1:n.1716+263_1716+264insG