Canonical Allele Identifier: CA358946417

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209764T>G (hg19) ; chr4:g.186288610T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288610T>G , CM000666.2:g.186288610T>G	GRCh38
NC_000004.11:g.187209764T>G , CM000666.1:g.187209764T>G	GRCh37
NC_000004.10:g.187446758T>G	NCBI36
NG_008051.1:g.27647T>G , LRG_583:g.27647T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1874T>G (F11) MANE Select	ENSP00000384957.2:p.Val625Gly
ENST00000264691.4:c.474T>G (F11)
ENST00000264692.8:c.1712T>G (F11)	ENSP00000264692.5:p.Val571Gly
ENST00000403665.6:c.1874T>G (F11)	ENSP00000384957.2:p.Val625Gly
ENST00000503841.1:n.393T>G (F11)
NM_000128.3:c.1874T>G , LRG_583t1:c.1874T>G (F11)	NP_000119.1:p.Val625Gly
NR_033900.1:n.884A>C (F11-AS1)
XM_005262821.2:c.1877T>G (F11)	XP_005262878.1:p.Val626Gly
XM_005262822.2:c.1781T>G (F11)	XP_005262879.1:p.Val594Gly
XM_005262823.2:c.1607T>G (F11)	XP_005262880.1:p.Val536Gly
XM_006714137.1:c.1829T>G (F11)	XP_006714200.1:p.Val610Gly
XM_005262821.4:c.1877T>G (F11)	XP_005262878.1:p.Val626Gly
XM_005262822.4:c.1781T>G (F11)	XP_005262879.1:p.Val594Gly
XM_005262823.4:c.1607T>G (F11)	XP_005262880.1:p.Val536Gly
XM_006714137.3:c.1829T>G (F11)	XP_006714200.1:p.Val610Gly
NM_000128.4:c.1874T>G (F11) MANE Select	NP_000119.1:p.Val625Gly