Canonical Allele Identifier: CA1519939339

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287592_186287593delinsAT , CM000666.2:g.186287592_186287593delinsAT	GRCh38
NC_000004.11:g.187208746_187208747delinsAT , CM000666.1:g.187208746_187208747delinsAT	GRCh37
NC_000004.10:g.187445740_187445741delinsAT	NCBI36
NG_008051.1:g.26629_26630delinsAT , LRG_583:g.26629_26630delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1577-92_1577-91delinsAT (F11) MANE Select	ENSP00000384957.2:n.1577-92_1577-91delinsAT
ENST00000264691.4:c.177-92_177-91delinsAT (F11)
ENST00000264692.8:c.1415-92_1415-91delinsAT (F11)	ENSP00000264692.5:n.1415-92_1415-91delinsAT
ENST00000403665.6:c.1577-92_1577-91delinsAT (F11)	ENSP00000384957.2:n.1577-92_1577-91delinsAT
ENST00000503841.1:n.4_5delinsAT (F11)
NM_000128.3:c.1577-92_1577-91delinsAT , LRG_583t1:c.1577-92_1577-91delinsAT (F11)	NP_000119.1:n.1577-92_1577-91delinsAT
NR_033900.1:n.1066+835_1066+836delinsAT (F11-AS1)
XM_005262821.2:c.1580-92_1580-91delinsAT (F11)	XP_005262878.1:n.1580-92_1580-91delinsAT
XM_005262822.2:c.1484-92_1484-91delinsAT (F11)	XP_005262879.1:n.1484-92_1484-91delinsAT
XM_005262823.2:c.1310-92_1310-91delinsAT (F11)	XP_005262880.1:n.1310-92_1310-91delinsAT
XM_006714137.1:c.1532-92_1532-91delinsAT (F11)	XP_006714200.1:n.1532-92_1532-91delinsAT
XR_938706.1:n.1985-92_1985-91delinsAT (F11)
XR_938707.1:n.1889-92_1889-91delinsAT (F11)
XM_005262821.4:c.1580-92_1580-91delinsAT (F11)	XP_005262878.1:n.1580-92_1580-91delinsAT
XM_005262822.4:c.1484-92_1484-91delinsAT (F11)	XP_005262879.1:n.1484-92_1484-91delinsAT
XM_005262823.4:c.1310-92_1310-91delinsAT (F11)	XP_005262880.1:n.1310-92_1310-91delinsAT
XM_006714137.3:c.1532-92_1532-91delinsAT (F11)	XP_006714200.1:n.1532-92_1532-91delinsAT
NM_000128.4:c.1577-92_1577-91delinsAT (F11) MANE Select	NP_000119.1:n.1577-92_1577-91delinsAT