Canonical Allele Identifier: CA442641168

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186287796-C-T
• MyVariant Identifiers: chr4:g.187208950C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287796C>T , CM000666.2:g.186287796C>T	GRCh38
NC_000004.11:g.187208950C>T , CM000666.1:g.187208950C>T	GRCh37
NC_000004.10:g.187445944C>T	NCBI36
NG_008051.1:g.26833C>T , LRG_583:g.26833C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1689C>T (F11) MANE Select	ENSP00000384957.2:p.Tyr563=
ENST00000264691.4:c.289C>T (F11)
ENST00000264692.8:c.1527C>T (F11)	ENSP00000264692.5:p.Tyr509=
ENST00000403665.6:c.1689C>T (F11)	ENSP00000384957.2:p.Tyr563=
ENST00000503841.1:n.208C>T (F11)
NM_000128.3:c.1689C>T , LRG_583t1:c.1689C>T (F11)	NP_000119.1:p.Tyr563=
NR_033900.1:n.1066+632G>A (F11-AS1)
XM_005262821.2:c.1692C>T (F11)	XP_005262878.1:p.Tyr564=
XM_005262822.2:c.1596C>T (F11)	XP_005262879.1:p.Tyr532=
XM_005262823.2:c.1422C>T (F11)	XP_005262880.1:p.Tyr474=
XM_006714137.1:c.1644C>T (F11)	XP_006714200.1:p.Tyr548=
XM_005262821.4:c.1692C>T (F11)	XP_005262878.1:p.Tyr564=
XM_005262822.4:c.1596C>T (F11)	XP_005262879.1:p.Tyr532=
XM_005262823.4:c.1422C>T (F11)	XP_005262880.1:p.Tyr474=
XM_006714137.3:c.1644C>T (F11)	XP_006714200.1:p.Tyr548=
NM_000128.4:c.1689C>T (F11) MANE Select	NP_000119.1:p.Tyr563=