Canonical Allele Identifier: CA1519939493

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287889_186287891delinsTTG , CM000666.2:g.186287889_186287891delinsTTG	GRCh38
NC_000004.11:g.187209043_187209045delinsTTG , CM000666.1:g.187209043_187209045delinsTTG	GRCh37
NC_000004.10:g.187446037_187446039delinsTTG	NCBI36
NG_008051.1:g.26926_26928delinsTTG , LRG_583:g.26926_26928delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+66_1716+68delinsTTG (F11) MANE Select	ENSP00000384957.2:n.1716+66_1716+68delinsTTG
ENST00000264691.4:c.316+66_316+68delinsTTG (F11)
ENST00000264692.8:c.1554+66_1554+68delinsTTG (F11)	ENSP00000264692.5:n.1554+66_1554+68delinsTTG
ENST00000403665.6:c.1716+66_1716+68delinsTTG (F11)	ENSP00000384957.2:n.1716+66_1716+68delinsTTG
ENST00000503841.1:n.235+66_235+68delinsTTG (F11)
NM_000128.3:c.1716+66_1716+68delinsTTG , LRG_583t1:c.1716+66_1716+68delinsTTG (F11)	NP_000119.1:n.1716+66_1716+68delinsTTG
NR_033900.1:n.1066+537_1066+539delinsCAA (F11-AS1)
XM_005262821.2:c.1719+66_1719+68delinsTTG (F11)	XP_005262878.1:n.1719+66_1719+68delinsTTG
XM_005262822.2:c.1623+66_1623+68delinsTTG (F11)	XP_005262879.1:n.1623+66_1623+68delinsTTG
XM_005262823.2:c.1449+66_1449+68delinsTTG (F11)	XP_005262880.1:n.1449+66_1449+68delinsTTG
XM_006714137.1:c.1671+66_1671+68delinsTTG (F11)	XP_006714200.1:n.1671+66_1671+68delinsTTG
XM_005262821.4:c.1719+66_1719+68delinsTTG (F11)	XP_005262878.1:n.1719+66_1719+68delinsTTG
XM_005262822.4:c.1623+66_1623+68delinsTTG (F11)	XP_005262879.1:n.1623+66_1623+68delinsTTG
XM_005262823.4:c.1449+66_1449+68delinsTTG (F11)	XP_005262880.1:n.1449+66_1449+68delinsTTG
XM_006714137.3:c.1671+66_1671+68delinsTTG (F11)	XP_006714200.1:n.1671+66_1671+68delinsTTG
NM_000128.4:c.1716+66_1716+68delinsTTG (F11) MANE Select	NP_000119.1:n.1716+66_1716+68delinsTTG