Canonical Allele Identifier: CA1071927834

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1741325816
• gnomAD v3: 4-186287857-C-G
• gnomAD v4: 4-186287857-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287857C>G , CM000666.2:g.186287857C>G	GRCh38
NC_000004.11:g.187209011C>G , CM000666.1:g.187209011C>G	GRCh37
NC_000004.10:g.187446005C>G	NCBI36
NG_008051.1:g.26894C>G , LRG_583:g.26894C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1716+34C>G (F11) MANE Select	ENSP00000384957.2:n.1716+34C>G
ENST00000264691.4:c.316+34C>G (F11)
ENST00000264692.8:c.1554+34C>G (F11)	ENSP00000264692.5:n.1554+34C>G
ENST00000403665.6:c.1716+34C>G (F11)	ENSP00000384957.2:n.1716+34C>G
ENST00000503841.1:n.235+34C>G (F11)
NM_000128.3:c.1716+34C>G , LRG_583t1:c.1716+34C>G (F11)	NP_000119.1:n.1716+34C>G
NR_033900.1:n.1066+571G>C (F11-AS1)
XM_005262821.2:c.1719+34C>G (F11)	XP_005262878.1:n.1719+34C>G
XM_005262822.2:c.1623+34C>G (F11)	XP_005262879.1:n.1623+34C>G
XM_005262823.2:c.1449+34C>G (F11)	XP_005262880.1:n.1449+34C>G
XM_006714137.1:c.1671+34C>G (F11)	XP_006714200.1:n.1671+34C>G
XM_005262821.4:c.1719+34C>G (F11)	XP_005262878.1:n.1719+34C>G
XM_005262822.4:c.1623+34C>G (F11)	XP_005262879.1:n.1623+34C>G
XM_005262823.4:c.1449+34C>G (F11)	XP_005262880.1:n.1449+34C>G
XM_006714137.3:c.1671+34C>G (F11)	XP_006714200.1:n.1671+34C>G
NM_000128.4:c.1716+34C>G (F11) MANE Select	NP_000119.1:n.1716+34C>G