Canonical Allele Identifier: CA1519939518

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287908_186287909delinsTG , CM000666.2:g.186287908_186287909delinsTG	GRCh38
NC_000004.11:g.187209062_187209063delinsTG , CM000666.1:g.187209062_187209063delinsTG	GRCh37
NC_000004.10:g.187446056_187446057delinsTG	NCBI36
NG_008051.1:g.26945_26946delinsTG , LRG_583:g.26945_26946delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+85_1716+86delinsTG (F11) MANE Select	ENSP00000384957.2:n.1716+85_1716+86delinsTG
ENST00000264691.4:c.316+85_316+86delinsTG (F11)
ENST00000264692.8:c.1554+85_1554+86delinsTG (F11)	ENSP00000264692.5:n.1554+85_1554+86delinsTG
ENST00000403665.6:c.1716+85_1716+86delinsTG (F11)	ENSP00000384957.2:n.1716+85_1716+86delinsTG
ENST00000503841.1:n.235+85_235+86delinsTG (F11)
NM_000128.3:c.1716+85_1716+86delinsTG , LRG_583t1:c.1716+85_1716+86delinsTG (F11)	NP_000119.1:n.1716+85_1716+86delinsTG
NR_033900.1:n.1066+519_1066+520delinsCA (F11-AS1)
XM_005262821.2:c.1719+85_1719+86delinsTG (F11)	XP_005262878.1:n.1719+85_1719+86delinsTG
XM_005262822.2:c.1623+85_1623+86delinsTG (F11)	XP_005262879.1:n.1623+85_1623+86delinsTG
XM_005262823.2:c.1449+85_1449+86delinsTG (F11)	XP_005262880.1:n.1449+85_1449+86delinsTG
XM_006714137.1:c.1671+85_1671+86delinsTG (F11)	XP_006714200.1:n.1671+85_1671+86delinsTG
XM_005262821.4:c.1719+85_1719+86delinsTG (F11)	XP_005262878.1:n.1719+85_1719+86delinsTG
XM_005262822.4:c.1623+85_1623+86delinsTG (F11)	XP_005262879.1:n.1623+85_1623+86delinsTG
XM_005262823.4:c.1449+85_1449+86delinsTG (F11)	XP_005262880.1:n.1449+85_1449+86delinsTG
XM_006714137.3:c.1671+85_1671+86delinsTG (F11)	XP_006714200.1:n.1671+85_1671+86delinsTG
NM_000128.4:c.1716+85_1716+86delinsTG (F11) MANE Select	NP_000119.1:n.1716+85_1716+86delinsTG