Canonical Allele Identifier: CA2672901637

Gene: F11

Linked Data

• gnomAD v4: 4-186274404-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274404C>G , CM000666.2:g.186274404C>G	GRCh38
NC_000004.11:g.187195558C>G , CM000666.1:g.187195558C>G	GRCh37
NC_000004.10:g.187432552C>G	NCBI36
NG_008051.1:g.13441C>G , LRG_583:g.13441C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.485+129C>G MANE Select	ENSP00000384957.2:n.485+129C>G
ENST00000264692.8:c.323+1229C>G	ENSP00000264692.5:n.323+1229C>G
ENST00000403665.6:c.485+129C>G	ENSP00000384957.2:n.485+129C>G
ENST00000492972.6:c.*125C>G	ENSP00000424479.1:n.*125C>G
ENST00000514715.1:n.486C>G
NM_000128.3:c.485+129C>G , LRG_583t1:c.485+129C>G	NP_000119.1:n.485+129C>G
XM_005262821.2:c.485+129C>G	XP_005262878.1:n.485+129C>G
XM_005262822.2:c.485+129C>G	XP_005262879.1:n.485+129C>G
XM_005262823.2:c.485+129C>G	XP_005262880.1:n.485+129C>G
XM_005262824.1:c.485+129C>G	XP_005262881.1:n.485+129C>G
XM_006714137.1:c.485+129C>G	XP_006714200.1:n.485+129C>G
XR_938706.1:n.837+129C>G
XR_938707.1:n.837+129C>G
NM_001354804.1:c.*125C>G	NP_001341733.1:n.*125C>G
XM_005262821.4:c.485+129C>G	XP_005262878.1:n.485+129C>G
XM_005262822.4:c.485+129C>G	XP_005262879.1:n.485+129C>G
XM_005262823.4:c.485+129C>G	XP_005262880.1:n.485+129C>G
XM_006714137.3:c.485+129C>G	XP_006714200.1:n.485+129C>G
XM_017007884.2:c.485+129C>G	XP_016863373.1:n.485+129C>G
XM_017007885.2:c.485+129C>G	XP_016863374.1:n.485+129C>G
XM_017007886.2:c.485+129C>G	XP_016863375.1:n.485+129C>G
XR_001741172.2:n.818+129C>G
NM_000128.4:c.485+129C>G MANE Select	NP_000119.1:n.485+129C>G
NM_001354804.2:c.*125C>G	NP_001341733.1:n.*125C>G