Canonical Allele Identifier: CA358944005

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187207593C>G (hg19) ; chr4:g.186286439C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286439C>G , CM000666.2:g.186286439C>G	GRCh38
NC_000004.11:g.187207593C>G , CM000666.1:g.187207593C>G	GRCh37
NC_000004.10:g.187444587C>G	NCBI36
NG_008051.1:g.25476C>G , LRG_583:g.25476C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1505C>G (F11) MANE Select	ENSP00000384957.2:p.Pro502Arg
ENST00000264691.4:c.176+626C>G (F11)
ENST00000264692.8:c.1343C>G (F11)	ENSP00000264692.5:p.Pro448Arg
ENST00000403665.6:c.1505C>G (F11)	ENSP00000384957.2:p.Pro502Arg
NM_000128.3:c.1505C>G , LRG_583t1:c.1505C>G (F11)	NP_000119.1:p.Pro502Arg
NR_033900.1:n.1067-173G>C (F11-AS1)
XM_005262821.2:c.1508C>G (F11)	XP_005262878.1:p.Pro503Arg
XM_005262822.2:c.1483+626C>G (F11)	XP_005262879.1:n.1483+626C>G
XM_005262823.2:c.1238C>G (F11)	XP_005262880.1:p.Pro413Arg
XM_005262824.1:c.1484-107C>G (F11)	XP_005262881.1:n.1484-107C>G
XM_006714137.1:c.1460C>G (F11)	XP_006714200.1:p.Pro487Arg
XR_938706.1:n.1913C>G (F11)
XR_938707.1:n.1888+626C>G (F11)
XM_005262821.4:c.1508C>G (F11)	XP_005262878.1:p.Pro503Arg
XM_005262822.4:c.1483+626C>G (F11)	XP_005262879.1:n.1483+626C>G
XM_005262823.4:c.1238C>G (F11)	XP_005262880.1:p.Pro413Arg
XM_006714137.3:c.1460C>G (F11)	XP_006714200.1:p.Pro487Arg
XR_001741172.2:n.1979C>G (F11)
NM_000128.4:c.1505C>G (F11) MANE Select	NP_000119.1:p.Pro502Arg