Canonical Allele Identifier: CA112104111

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs922669321
• gnomAD v3: 4-186286239-C-T
• gnomAD v4: 4-186286239-C-T
• MyVariant Identifiers: chr4:g.187207393C>T (hg19) ; chr4:g.186286239C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286239C>T , CM000666.2:g.186286239C>T	GRCh38
NC_000004.11:g.187207393C>T , CM000666.1:g.187207393C>T	GRCh37
NC_000004.10:g.187444387C>T	NCBI36
NG_008051.1:g.25276C>T , LRG_583:g.25276C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1481-176C>T (F11) MANE Select	ENSP00000384957.2:n.1481-176C>T
ENST00000264691.4:c.176+426C>T (F11)
ENST00000264692.8:c.1319-176C>T (F11)	ENSP00000264692.5:n.1319-176C>T
ENST00000403665.6:c.1481-176C>T (F11)	ENSP00000384957.2:n.1481-176C>T
NM_000128.3:c.1481-176C>T , LRG_583t1:c.1481-176C>T (F11)	NP_000119.1:n.1481-176C>T
NR_033900.1:n.1094G>A (F11-AS1)
XM_005262821.2:c.1484-176C>T (F11)	XP_005262878.1:n.1484-176C>T
XM_005262822.2:c.1483+426C>T (F11)	XP_005262879.1:n.1483+426C>T
XM_005262823.2:c.1214-176C>T (F11)	XP_005262880.1:n.1214-176C>T
XM_005262824.1:c.1484-307C>T (F11)	XP_005262881.1:n.1484-307C>T
XM_006714137.1:c.1436-176C>T (F11)	XP_006714200.1:n.1436-176C>T
XR_938706.1:n.1889-176C>T (F11)
XR_938707.1:n.1888+426C>T (F11)
XM_005262821.4:c.1484-176C>T (F11)	XP_005262878.1:n.1484-176C>T
XM_005262822.4:c.1483+426C>T (F11)	XP_005262879.1:n.1483+426C>T
XM_005262823.4:c.1214-176C>T (F11)	XP_005262880.1:n.1214-176C>T
XM_006714137.3:c.1436-176C>T (F11)	XP_006714200.1:n.1436-176C>T
XR_001741172.2:n.1955-176C>T (F11)
NM_000128.4:c.1481-176C>T (F11) MANE Select	NP_000119.1:n.1481-176C>T