Canonical Allele Identifier: CA358959206

Gene: F11

Linked Data

• ClinVar Variation Id: 552592
• ClinVar RCV Id: RCV000667883
• dbSNP Id: rs1489595409
• gnomAD v2: 4-187197469-G-A
• gnomAD v3: 4-186276315-G-A
• gnomAD v4: 4-186276315-G-A
• MyVariant Identifiers: chr4:g.187197469G>A (hg19) ; chr4:g.186276315G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276315G>A , CM000666.2:g.186276315G>A	GRCh38
NC_000004.11:g.187197469G>A , CM000666.1:g.187197469G>A	GRCh37
NC_000004.10:g.187434463G>A	NCBI36
NG_008051.1:g.15352G>A , LRG_583:g.15352G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.680G>A MANE Select	ENSP00000384957.2:p.Gly227Asp
ENST00000264692.8:c.518G>A	ENSP00000264692.5:p.Gly173Asp
ENST00000403665.6:c.680G>A	ENSP00000384957.2:p.Gly227Asp
ENST00000452239.1:c.127G>A
NM_000128.3:c.680G>A , LRG_583t1:c.680G>A	NP_000119.1:p.Gly227Asp
XM_005262821.2:c.680G>A	XP_005262878.1:p.Gly227Asp
XM_005262822.2:c.680G>A	XP_005262879.1:p.Gly227Asp
XM_005262823.2:c.485+2040G>A	XP_005262880.1:n.485+2040G>A
XM_005262824.1:c.680G>A	XP_005262881.1:p.Gly227Asp
XM_006714137.1:c.680G>A	XP_006714200.1:p.Gly227Asp
XR_938706.1:n.1032G>A
XR_938707.1:n.1032G>A
XM_005262821.4:c.680G>A	XP_005262878.1:p.Gly227Asp
XM_005262822.4:c.680G>A	XP_005262879.1:p.Gly227Asp
XM_005262823.4:c.485+2040G>A	XP_005262880.1:n.485+2040G>A
XM_006714137.3:c.680G>A	XP_006714200.1:p.Gly227Asp
XM_017007884.2:c.680G>A	XP_016863373.1:p.Gly227Asp
XM_017007885.2:c.680G>A	XP_016863374.1:p.Gly227Asp
XM_017007886.2:c.680G>A	XP_016863375.1:p.Gly227Asp
XR_001741172.2:n.1013G>A
NM_000128.4:c.680G>A MANE Select	NP_000119.1:p.Gly227Asp