Canonical Allele Identifier: CA442644279

Gene: F11

Linked Data

• gnomAD v4: 4-186274207-A-G
• MyVariant Identifiers: chr4:g.187195361A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274207A>G , CM000666.2:g.186274207A>G	GRCh38
NC_000004.11:g.187195361A>G , CM000666.1:g.187195361A>G	GRCh37
NC_000004.10:g.187432355A>G	NCBI36
NG_008051.1:g.13244A>G , LRG_583:g.13244A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.417A>G MANE Select	ENSP00000384957.2:p.Arg139=
ENST00000264692.8:c.323+1032A>G	ENSP00000264692.5:n.323+1032A>G
ENST00000403665.6:c.417A>G	ENSP00000384957.2:p.Arg139=
ENST00000492972.6:c.417A>G	ENSP00000424479.1:p.Arg139=
ENST00000514715.1:n.289A>G
NM_000128.3:c.417A>G , LRG_583t1:c.417A>G	NP_000119.1:p.Arg139=
XM_005262821.2:c.417A>G	XP_005262878.1:p.Arg139=
XM_005262822.2:c.417A>G	XP_005262879.1:p.Arg139=
XM_005262823.2:c.417A>G	XP_005262880.1:p.Arg139=
XM_005262824.1:c.417A>G	XP_005262881.1:p.Arg139=
XM_006714137.1:c.417A>G	XP_006714200.1:p.Arg139=
XR_938706.1:n.769A>G
XR_938707.1:n.769A>G
NM_001354804.1:c.417A>G	NP_001341733.1:p.Arg139=
XM_005262821.4:c.417A>G	XP_005262878.1:p.Arg139=
XM_005262822.4:c.417A>G	XP_005262879.1:p.Arg139=
XM_005262823.4:c.417A>G	XP_005262880.1:p.Arg139=
XM_006714137.3:c.417A>G	XP_006714200.1:p.Arg139=
XM_017007884.2:c.417A>G	XP_016863373.1:p.Arg139=
XM_017007885.2:c.417A>G	XP_016863374.1:p.Arg139=
XM_017007886.2:c.417A>G	XP_016863375.1:p.Arg139=
XR_001741172.2:n.750A>G
NM_000128.4:c.417A>G MANE Select	NP_000119.1:p.Arg139=
NM_001354804.2:c.417A>G	NP_001341733.1:p.Arg139=