Canonical Allele Identifier: CA358946267

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1741389510
• gnomAD v3: 4-186288576-T-G
• gnomAD v4: 4-186288576-T-G
• MyVariant Identifiers: chr4:g.187209730T>G (hg19) ; chr4:g.186288576T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288576T>G , CM000666.2:g.186288576T>G	GRCh38
NC_000004.11:g.187209730T>G , CM000666.1:g.187209730T>G	GRCh37
NC_000004.10:g.187446724T>G	NCBI36
NG_008051.1:g.27613T>G , LRG_583:g.27613T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1840T>G (F11) MANE Select	ENSP00000384957.2:p.Tyr614Asp
ENST00000264691.4:c.440T>G (F11)
ENST00000264692.8:c.1678T>G (F11)	ENSP00000264692.5:p.Tyr560Asp
ENST00000403665.6:c.1840T>G (F11)	ENSP00000384957.2:p.Tyr614Asp
ENST00000503841.1:n.359T>G (F11)
NM_000128.3:c.1840T>G , LRG_583t1:c.1840T>G (F11)	NP_000119.1:p.Tyr614Asp
NR_033900.1:n.918A>C (F11-AS1)
XM_005262821.2:c.1843T>G (F11)	XP_005262878.1:p.Tyr615Asp
XM_005262822.2:c.1747T>G (F11)	XP_005262879.1:p.Tyr583Asp
XM_005262823.2:c.1573T>G (F11)	XP_005262880.1:p.Tyr525Asp
XM_006714137.1:c.1795T>G (F11)	XP_006714200.1:p.Tyr599Asp
XM_005262821.4:c.1843T>G (F11)	XP_005262878.1:p.Tyr615Asp
XM_005262822.4:c.1747T>G (F11)	XP_005262879.1:p.Tyr583Asp
XM_005262823.4:c.1573T>G (F11)	XP_005262880.1:p.Tyr525Asp
XM_006714137.3:c.1795T>G (F11)	XP_006714200.1:p.Tyr599Asp
NM_000128.4:c.1840T>G (F11) MANE Select	NP_000119.1:p.Tyr614Asp