Canonical Allele Identifier: CA1519939609

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288084_186288089delinsTTTTAG , CM000666.2:g.186288084_186288089delinsTTTTAG	GRCh38
NC_000004.11:g.187209238_187209243delinsTTTTAG , CM000666.1:g.187209238_187209243delinsTTTTAG	GRCh37
NC_000004.10:g.187446232_187446237delinsTTTTAG	NCBI36
NG_008051.1:g.27121_27126delinsTTTTAG , LRG_583:g.27121_27126delinsTTTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+261_1716+266delinsTTTTAG (F11) MANE Select	ENSP00000384957.2:n.1716+261_1716+266delinsTTTTAG
ENST00000264691.4:c.316+261_316+266delinsTTTTAG (F11)
ENST00000264692.8:c.1554+261_1554+266delinsTTTTAG (F11)	ENSP00000264692.5:n.1554+261_1554+266delinsTTTTAG
ENST00000403665.6:c.1716+261_1716+266delinsTTTTAG (F11)	ENSP00000384957.2:n.1716+261_1716+266delinsTTTTAG
ENST00000503841.1:n.235+261_235+266delinsTTTTAG (F11)
NM_000128.3:c.1716+261_1716+266delinsTTTTAG , LRG_583t1:c.1716+261_1716+266delinsTTTTAG (F11)	NP_000119.1:n.1716+261_1716+266delinsTTTTAG
NR_033900.1:n.1066+339_1066+344delinsCTAAAA (F11-AS1)
XM_005262821.2:c.1719+261_1719+266delinsTTTTAG (F11)	XP_005262878.1:n.1719+261_1719+266delinsTTTTAG
XM_005262822.2:c.1623+261_1623+266delinsTTTTAG (F11)	XP_005262879.1:n.1623+261_1623+266delinsTTTTAG
XM_005262823.2:c.1449+261_1449+266delinsTTTTAG (F11)	XP_005262880.1:n.1449+261_1449+266delinsTTTTAG
XM_006714137.1:c.1671+261_1671+266delinsTTTTAG (F11)	XP_006714200.1:n.1671+261_1671+266delinsTTTTAG
XM_005262821.4:c.1719+261_1719+266delinsTTTTAG (F11)	XP_005262878.1:n.1719+261_1719+266delinsTTTTAG
XM_005262822.4:c.1623+261_1623+266delinsTTTTAG (F11)	XP_005262879.1:n.1623+261_1623+266delinsTTTTAG
XM_005262823.4:c.1449+261_1449+266delinsTTTTAG (F11)	XP_005262880.1:n.1449+261_1449+266delinsTTTTAG
XM_006714137.3:c.1671+261_1671+266delinsTTTTAG (F11)	XP_006714200.1:n.1671+261_1671+266delinsTTTTAG
NM_000128.4:c.1716+261_1716+266delinsTTTTAG (F11) MANE Select	NP_000119.1:n.1716+261_1716+266delinsTTTTAG