Canonical Allele Identifier: CA358943602

Gene: F11

Linked Data

• gnomAD v4: 4-186285773-T-G
• MyVariant Identifiers: chr4:g.187206927T>G (hg19) ; chr4:g.186285773T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285773T>G , CM000666.2:g.186285773T>G	GRCh38
NC_000004.11:g.187206927T>G , CM000666.1:g.187206927T>G	GRCh37
NC_000004.10:g.187443921T>G	NCBI36
NG_008051.1:g.24810T>G , LRG_583:g.24810T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1440T>G MANE Select	ENSP00000384957.2:p.Asp480Glu
ENST00000264691.4:c.136T>G
ENST00000264692.8:c.1278T>G	ENSP00000264692.5:p.Asp426Glu
ENST00000403665.6:c.1440T>G	ENSP00000384957.2:p.Asp480Glu
NM_000128.3:c.1440T>G , LRG_583t1:c.1440T>G	NP_000119.1:p.Asp480Glu
XM_005262821.2:c.1443T>G	XP_005262878.1:p.Asp481Glu
XM_005262822.2:c.1443T>G	XP_005262879.1:p.Asp481Glu
XM_005262823.2:c.1173T>G	XP_005262880.1:p.Asp391Glu
XM_005262824.1:c.1443T>G	XP_005262881.1:p.Asp481Glu
XM_006714137.1:c.1395T>G	XP_006714200.1:p.Asp465Glu
XR_938706.1:n.1848T>G
XR_938707.1:n.1848T>G
XM_005262821.4:c.1443T>G	XP_005262878.1:p.Asp481Glu
XM_005262822.4:c.1443T>G	XP_005262879.1:p.Asp481Glu
XM_005262823.4:c.1173T>G	XP_005262880.1:p.Asp391Glu
XM_006714137.3:c.1395T>G	XP_006714200.1:p.Asp465Glu
XR_001741172.2:n.1914T>G
NM_000128.4:c.1440T>G MANE Select	NP_000119.1:p.Asp480Glu