Canonical Allele Identifier: CA358946050

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209665T>C (hg19) ; chr4:g.186288511T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288511T>C , CM000666.2:g.186288511T>C	GRCh38
NC_000004.11:g.187209665T>C , CM000666.1:g.187209665T>C	GRCh37
NC_000004.10:g.187446659T>C	NCBI36
NG_008051.1:g.27548T>C , LRG_583:g.27548T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1775T>C (F11) MANE Select	ENSP00000384957.2:p.Ile592Thr
ENST00000264691.4:c.375T>C (F11)
ENST00000264692.8:c.1613T>C (F11)	ENSP00000264692.5:p.Ile538Thr
ENST00000403665.6:c.1775T>C (F11)	ENSP00000384957.2:p.Ile592Thr
ENST00000503841.1:n.294T>C (F11)
NM_000128.3:c.1775T>C , LRG_583t1:c.1775T>C (F11)	NP_000119.1:p.Ile592Thr
NR_033900.1:n.983A>G (F11-AS1)
XM_005262821.2:c.1778T>C (F11)	XP_005262878.1:p.Ile593Thr
XM_005262822.2:c.1682T>C (F11)	XP_005262879.1:p.Ile561Thr
XM_005262823.2:c.1508T>C (F11)	XP_005262880.1:p.Ile503Thr
XM_006714137.1:c.1730T>C (F11)	XP_006714200.1:p.Ile577Thr
XM_005262821.4:c.1778T>C (F11)	XP_005262878.1:p.Ile593Thr
XM_005262822.4:c.1682T>C (F11)	XP_005262879.1:p.Ile561Thr
XM_005262823.4:c.1508T>C (F11)	XP_005262880.1:p.Ile503Thr
XM_006714137.3:c.1730T>C (F11)	XP_006714200.1:p.Ile577Thr
NM_000128.4:c.1775T>C (F11) MANE Select	NP_000119.1:p.Ile592Thr