Canonical Allele Identifier: CA358941624

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205274C>G (hg19) ; chr4:g.186284120C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284120C>G , CM000666.2:g.186284120C>G	GRCh38
NC_000004.11:g.187205274C>G , CM000666.1:g.187205274C>G	GRCh37
NC_000004.10:g.187442268C>G	NCBI36
NG_008051.1:g.23157C>G , LRG_583:g.23157C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1164C>G MANE Select	ENSP00000384957.2:p.Ile388Met
ENST00000264692.8:c.1002C>G	ENSP00000264692.5:p.Ile334Met
ENST00000403665.6:c.1164C>G	ENSP00000384957.2:p.Ile388Met
NM_000128.3:c.1164C>G , LRG_583t1:c.1164C>G	NP_000119.1:p.Ile388Met
XM_005262821.2:c.1167C>G	XP_005262878.1:p.Ile389Met
XM_005262822.2:c.1167C>G	XP_005262879.1:p.Ile389Met
XM_005262823.2:c.897C>G	XP_005262880.1:p.Ile299Met
XM_005262824.1:c.1167C>G	XP_005262881.1:p.Ile389Met
XM_006714137.1:c.1119C>G	XP_006714200.1:p.Ile373Met
XR_938706.1:n.1572C>G
XR_938707.1:n.1572C>G
XM_005262821.4:c.1167C>G	XP_005262878.1:p.Ile389Met
XM_005262822.4:c.1167C>G	XP_005262879.1:p.Ile389Met
XM_005262823.4:c.897C>G	XP_005262880.1:p.Ile299Met
XM_006714137.3:c.1119C>G	XP_006714200.1:p.Ile373Met
XM_017007884.2:c.*2136C>G	XP_016863373.1:n.*2136C>G
XM_017007885.2:c.*32C>G	XP_016863374.1:n.*32C>G
XR_001741172.2:n.1638C>G
NM_000128.4:c.1164C>G MANE Select	NP_000119.1:p.Ile388Met