Canonical Allele Identifier: CA1519939504

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1741329787
• gnomAD v4: 4-186287896-TTTTGTTTTTTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287909_186287921del , CM000666.2:g.186287909_186287921del	GRCh38
NC_000004.11:g.187209063_187209075del , CM000666.1:g.187209063_187209075del	GRCh37
NC_000004.10:g.187446057_187446069del	NCBI36
NG_008051.1:g.26946_26958del , LRG_583:g.26946_26958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+86_1716+98del (F11) MANE Select	ENSP00000384957.2:n.1716+86_1716+98del
ENST00000264691.4:c.316+86_316+98del (F11)
ENST00000264692.8:c.1554+86_1554+98del (F11)	ENSP00000264692.5:n.1554+86_1554+98del
ENST00000403665.6:c.1716+86_1716+98del (F11)	ENSP00000384957.2:n.1716+86_1716+98del
ENST00000503841.1:n.235+86_235+98del (F11)
NM_000128.3:c.1716+86_1716+98del , LRG_583t1:c.1716+86_1716+98del (F11)	NP_000119.1:n.1716+86_1716+98del
NR_033900.1:n.1066+519_1066+531del (F11-AS1)
XM_005262821.2:c.1719+86_1719+98del (F11)	XP_005262878.1:n.1719+86_1719+98del
XM_005262822.2:c.1623+86_1623+98del (F11)	XP_005262879.1:n.1623+86_1623+98del
XM_005262823.2:c.1449+86_1449+98del (F11)	XP_005262880.1:n.1449+86_1449+98del
XM_006714137.1:c.1671+86_1671+98del (F11)	XP_006714200.1:n.1671+86_1671+98del
XM_005262821.4:c.1719+86_1719+98del (F11)	XP_005262878.1:n.1719+86_1719+98del
XM_005262822.4:c.1623+86_1623+98del (F11)	XP_005262879.1:n.1623+86_1623+98del
XM_005262823.4:c.1449+86_1449+98del (F11)	XP_005262880.1:n.1449+86_1449+98del
XM_006714137.3:c.1671+86_1671+98del (F11)	XP_006714200.1:n.1671+86_1671+98del
NM_000128.4:c.1716+86_1716+98del (F11) MANE Select	NP_000119.1:n.1716+86_1716+98del