Canonical Allele Identifier: CA358946172

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209691C>G (hg19) ; chr4:g.186288537C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288537C>G , CM000666.2:g.186288537C>G	GRCh38
NC_000004.11:g.187209691C>G , CM000666.1:g.187209691C>G	GRCh37
NC_000004.10:g.187446685C>G	NCBI36
NG_008051.1:g.27574C>G , LRG_583:g.27574C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1801C>G (F11) MANE Select	ENSP00000384957.2:p.Gln601Glu
ENST00000264691.4:c.401C>G (F11)
ENST00000264692.8:c.1639C>G (F11)	ENSP00000264692.5:p.Gln547Glu
ENST00000403665.6:c.1801C>G (F11)	ENSP00000384957.2:p.Gln601Glu
ENST00000503841.1:n.320C>G (F11)
NM_000128.3:c.1801C>G , LRG_583t1:c.1801C>G (F11)	NP_000119.1:p.Gln601Glu
NR_033900.1:n.957G>C (F11-AS1)
XM_005262821.2:c.1804C>G (F11)	XP_005262878.1:p.Gln602Glu
XM_005262822.2:c.1708C>G (F11)	XP_005262879.1:p.Gln570Glu
XM_005262823.2:c.1534C>G (F11)	XP_005262880.1:p.Gln512Glu
XM_006714137.1:c.1756C>G (F11)	XP_006714200.1:p.Gln586Glu
XM_005262821.4:c.1804C>G (F11)	XP_005262878.1:p.Gln602Glu
XM_005262822.4:c.1708C>G (F11)	XP_005262879.1:p.Gln570Glu
XM_005262823.4:c.1534C>G (F11)	XP_005262880.1:p.Gln512Glu
XM_006714137.3:c.1756C>G (F11)	XP_006714200.1:p.Gln586Glu
NM_000128.4:c.1801C>G (F11) MANE Select	NP_000119.1:p.Gln601Glu