Canonical Allele Identifier: CA2672903943

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186287927-C-CTCTGTCTCAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287927_186287928insTCTGTCTCAAA , CM000666.2:g.186287927_186287928insTCTGTCTCAAA	GRCh38
NC_000004.11:g.187209081_187209082insTCTGTCTCAAA , CM000666.1:g.187209081_187209082insTCTGTCTCAAA	GRCh37
NC_000004.10:g.187446075_187446076insTCTGTCTCAAA	NCBI36
NG_008051.1:g.26964_26965insTCTGTCTCAAA , LRG_583:g.26964_26965insTCTGTCTCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+104_1716+105insTCTGTCTCAAA (F11) MANE Select	ENSP00000384957.2:n.1716+104_1716+105insTCTGTCTCAAA
ENST00000264691.4:c.316+104_316+105insTCTGTCTCAAA (F11)
ENST00000264692.8:c.1554+104_1554+105insTCTGTCTCAAA (F11)	ENSP00000264692.5:n.1554+104_1554+105insTCTGTCTCAAA
ENST00000403665.6:c.1716+104_1716+105insTCTGTCTCAAA (F11)	ENSP00000384957.2:n.1716+104_1716+105insTCTGTCTCAAA
ENST00000503841.1:n.235+104_235+105insTCTGTCTCAAA (F11)
NM_000128.3:c.1716+104_1716+105insTCTGTCTCAAA , LRG_583t1:c.1716+104_1716+105insTCTGTCTCAAA (F11)	NP_000119.1:n.1716+104_1716+105insTCTGTCTCAAA
NR_033900.1:n.1066+500_1066+501insTTTGAGACAGA (F11-AS1)
XM_005262821.2:c.1719+104_1719+105insTCTGTCTCAAA (F11)	XP_005262878.1:n.1719+104_1719+105insTCTGTCTCAAA
XM_005262822.2:c.1623+104_1623+105insTCTGTCTCAAA (F11)	XP_005262879.1:n.1623+104_1623+105insTCTGTCTCAAA
XM_005262823.2:c.1449+104_1449+105insTCTGTCTCAAA (F11)	XP_005262880.1:n.1449+104_1449+105insTCTGTCTCAAA
XM_006714137.1:c.1671+104_1671+105insTCTGTCTCAAA (F11)	XP_006714200.1:n.1671+104_1671+105insTCTGTCTCAAA
XM_005262821.4:c.1719+104_1719+105insTCTGTCTCAAA (F11)	XP_005262878.1:n.1719+104_1719+105insTCTGTCTCAAA
XM_005262822.4:c.1623+104_1623+105insTCTGTCTCAAA (F11)	XP_005262879.1:n.1623+104_1623+105insTCTGTCTCAAA
XM_005262823.4:c.1449+104_1449+105insTCTGTCTCAAA (F11)	XP_005262880.1:n.1449+104_1449+105insTCTGTCTCAAA
XM_006714137.3:c.1671+104_1671+105insTCTGTCTCAAA (F11)	XP_006714200.1:n.1671+104_1671+105insTCTGTCTCAAA
NM_000128.4:c.1716+104_1716+105insTCTGTCTCAAA (F11) MANE Select	NP_000119.1:n.1716+104_1716+105insTCTGTCTCAAA