Canonical Allele Identifier: CA1519939342

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287594_186287595delinsAT , CM000666.2:g.186287594_186287595delinsAT	GRCh38
NC_000004.11:g.187208748_187208749delinsAT , CM000666.1:g.187208748_187208749delinsAT	GRCh37
NC_000004.10:g.187445742_187445743delinsAT	NCBI36
NG_008051.1:g.26631_26632delinsAT , LRG_583:g.26631_26632delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1577-90_1577-89delinsAT (F11) MANE Select	ENSP00000384957.2:n.1577-90_1577-89delinsAT
ENST00000264691.4:c.177-90_177-89delinsAT (F11)
ENST00000264692.8:c.1415-90_1415-89delinsAT (F11)	ENSP00000264692.5:n.1415-90_1415-89delinsAT
ENST00000403665.6:c.1577-90_1577-89delinsAT (F11)	ENSP00000384957.2:n.1577-90_1577-89delinsAT
ENST00000503841.1:n.6_7delinsAT (F11)
NM_000128.3:c.1577-90_1577-89delinsAT , LRG_583t1:c.1577-90_1577-89delinsAT (F11)	NP_000119.1:n.1577-90_1577-89delinsAT
NR_033900.1:n.1066+833_1066+834delinsAT (F11-AS1)
XM_005262821.2:c.1580-90_1580-89delinsAT (F11)	XP_005262878.1:n.1580-90_1580-89delinsAT
XM_005262822.2:c.1484-90_1484-89delinsAT (F11)	XP_005262879.1:n.1484-90_1484-89delinsAT
XM_005262823.2:c.1310-90_1310-89delinsAT (F11)	XP_005262880.1:n.1310-90_1310-89delinsAT
XM_006714137.1:c.1532-90_1532-89delinsAT (F11)	XP_006714200.1:n.1532-90_1532-89delinsAT
XR_938706.1:n.1985-90_1985-89delinsAT (F11)
XR_938707.1:n.1889-90_1889-89delinsAT (F11)
XM_005262821.4:c.1580-90_1580-89delinsAT (F11)	XP_005262878.1:n.1580-90_1580-89delinsAT
XM_005262822.4:c.1484-90_1484-89delinsAT (F11)	XP_005262879.1:n.1484-90_1484-89delinsAT
XM_005262823.4:c.1310-90_1310-89delinsAT (F11)	XP_005262880.1:n.1310-90_1310-89delinsAT
XM_006714137.3:c.1532-90_1532-89delinsAT (F11)	XP_006714200.1:n.1532-90_1532-89delinsAT
NM_000128.4:c.1577-90_1577-89delinsAT (F11) MANE Select	NP_000119.1:n.1577-90_1577-89delinsAT