Canonical Allele Identifier: CA442641382

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209684C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288530C>A , CM000666.2:g.186288530C>A	GRCh38
NC_000004.11:g.187209684C>A , CM000666.1:g.187209684C>A	GRCh37
NC_000004.10:g.187446678C>A	NCBI36
NG_008051.1:g.27567C>A , LRG_583:g.27567C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1794C>A (F11) MANE Select	ENSP00000384957.2:p.Gly598=
ENST00000264691.4:c.394C>A (F11)
ENST00000264692.8:c.1632C>A (F11)	ENSP00000264692.5:p.Gly544=
ENST00000403665.6:c.1794C>A (F11)	ENSP00000384957.2:p.Gly598=
ENST00000503841.1:n.313C>A (F11)
NM_000128.3:c.1794C>A , LRG_583t1:c.1794C>A (F11)	NP_000119.1:p.Gly598=
NR_033900.1:n.964G>T (F11-AS1)
XM_005262821.2:c.1797C>A (F11)	XP_005262878.1:p.Gly599=
XM_005262822.2:c.1701C>A (F11)	XP_005262879.1:p.Gly567=
XM_005262823.2:c.1527C>A (F11)	XP_005262880.1:p.Gly509=
XM_006714137.1:c.1749C>A (F11)	XP_006714200.1:p.Gly583=
XM_005262821.4:c.1797C>A (F11)	XP_005262878.1:p.Gly599=
XM_005262822.4:c.1701C>A (F11)	XP_005262879.1:p.Gly567=
XM_005262823.4:c.1527C>A (F11)	XP_005262880.1:p.Gly509=
XM_006714137.3:c.1749C>A (F11)	XP_006714200.1:p.Gly583=
NM_000128.4:c.1794C>A (F11) MANE Select	NP_000119.1:p.Gly598=