Canonical Allele Identifier: CA112105631

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs965877577
• gnomAD v3: 4-186287883-GTTTT-G
• gnomAD v4: 4-186287883-GTTTT-G
• MyVariant Identifiers: chr4:g.187209038_187209041del (hg19) ; chr4:g.186287884_186287887del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287887_186287890del , CM000666.2:g.186287887_186287890del	GRCh38
NC_000004.11:g.187209041_187209044del , CM000666.1:g.187209041_187209044del	GRCh37
NC_000004.10:g.187446035_187446038del	NCBI36
NG_008051.1:g.26924_26927del , LRG_583:g.26924_26927del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1716+64_1716+67del (F11) MANE Select	ENSP00000384957.2:n.1716+64_1716+67del
ENST00000264691.4:c.316+64_316+67del (F11)
ENST00000264692.8:c.1554+64_1554+67del (F11)	ENSP00000264692.5:n.1554+64_1554+67del
ENST00000403665.6:c.1716+64_1716+67del (F11)	ENSP00000384957.2:n.1716+64_1716+67del
ENST00000503841.1:n.235+64_235+67del (F11)
NM_000128.3:c.1716+64_1716+67del , LRG_583t1:c.1716+64_1716+67del (F11)	NP_000119.1:n.1716+64_1716+67del
NR_033900.1:n.1066+541_1066+544del (F11-AS1)
XM_005262821.2:c.1719+64_1719+67del (F11)	XP_005262878.1:n.1719+64_1719+67del
XM_005262822.2:c.1623+64_1623+67del (F11)	XP_005262879.1:n.1623+64_1623+67del
XM_005262823.2:c.1449+64_1449+67del (F11)	XP_005262880.1:n.1449+64_1449+67del
XM_006714137.1:c.1671+64_1671+67del (F11)	XP_006714200.1:n.1671+64_1671+67del
XM_005262821.4:c.1719+64_1719+67del (F11)	XP_005262878.1:n.1719+64_1719+67del
XM_005262822.4:c.1623+64_1623+67del (F11)	XP_005262879.1:n.1623+64_1623+67del
XM_005262823.4:c.1449+64_1449+67del (F11)	XP_005262880.1:n.1449+64_1449+67del
XM_006714137.3:c.1671+64_1671+67del (F11)	XP_006714200.1:n.1671+64_1671+67del
NM_000128.4:c.1716+64_1716+67del (F11) MANE Select	NP_000119.1:n.1716+64_1716+67del