Canonical Allele Identifier: CA358946088

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209674G>C (hg19) ; chr4:g.186288520G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288520G>C , CM000666.2:g.186288520G>C	GRCh38
NC_000004.11:g.187209674G>C , CM000666.1:g.187209674G>C	GRCh37
NC_000004.10:g.187446668G>C	NCBI36
NG_008051.1:g.27557G>C , LRG_583:g.27557G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1784G>C (F11) MANE Select	ENSP00000384957.2:p.Trp595Ser
ENST00000264691.4:c.384G>C (F11)
ENST00000264692.8:c.1622G>C (F11)	ENSP00000264692.5:p.Trp541Ser
ENST00000403665.6:c.1784G>C (F11)	ENSP00000384957.2:p.Trp595Ser
ENST00000503841.1:n.303G>C (F11)
NM_000128.3:c.1784G>C , LRG_583t1:c.1784G>C (F11)	NP_000119.1:p.Trp595Ser
NR_033900.1:n.974C>G (F11-AS1)
XM_005262821.2:c.1787G>C (F11)	XP_005262878.1:p.Trp596Ser
XM_005262822.2:c.1691G>C (F11)	XP_005262879.1:p.Trp564Ser
XM_005262823.2:c.1517G>C (F11)	XP_005262880.1:p.Trp506Ser
XM_006714137.1:c.1739G>C (F11)	XP_006714200.1:p.Trp580Ser
XM_005262821.4:c.1787G>C (F11)	XP_005262878.1:p.Trp596Ser
XM_005262822.4:c.1691G>C (F11)	XP_005262879.1:p.Trp564Ser
XM_005262823.4:c.1517G>C (F11)	XP_005262880.1:p.Trp506Ser
XM_006714137.3:c.1739G>C (F11)	XP_006714200.1:p.Trp580Ser
NM_000128.4:c.1784G>C (F11) MANE Select	NP_000119.1:p.Trp595Ser