Canonical Allele Identifier: CA358946005

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1561493161
• MyVariant Identifiers: chr4:g.187209654T>A (hg19) ; chr4:g.186288500T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288500T>A , CM000666.2:g.186288500T>A	GRCh38
NC_000004.11:g.187209654T>A , CM000666.1:g.187209654T>A	GRCh37
NC_000004.10:g.187446648T>A	NCBI36
NG_008051.1:g.27537T>A , LRG_583:g.27537T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1764T>A (F11) MANE Select	ENSP00000384957.2:p.His588Gln
ENST00000264691.4:c.364T>A (F11)
ENST00000264692.8:c.1602T>A (F11)	ENSP00000264692.5:p.His534Gln
ENST00000403665.6:c.1764T>A (F11)	ENSP00000384957.2:p.His588Gln
ENST00000503841.1:n.283T>A (F11)
NM_000128.3:c.1764T>A , LRG_583t1:c.1764T>A (F11)	NP_000119.1:p.His588Gln
NR_033900.1:n.994A>T (F11-AS1)
XM_005262821.2:c.1767T>A (F11)	XP_005262878.1:p.His589Gln
XM_005262822.2:c.1671T>A (F11)	XP_005262879.1:p.His557Gln
XM_005262823.2:c.1497T>A (F11)	XP_005262880.1:p.His499Gln
XM_006714137.1:c.1719T>A (F11)	XP_006714200.1:p.His573Gln
XM_005262821.4:c.1767T>A (F11)	XP_005262878.1:p.His589Gln
XM_005262822.4:c.1671T>A (F11)	XP_005262879.1:p.His557Gln
XM_005262823.4:c.1497T>A (F11)	XP_005262880.1:p.His499Gln
XM_006714137.3:c.1719T>A (F11)	XP_006714200.1:p.His573Gln
NM_000128.4:c.1764T>A (F11) MANE Select	NP_000119.1:p.His588Gln