Canonical Allele Identifier: CA3164070

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs772866283
• ExAC: 4:187208924 A / G
• gnomAD v2: 4-187208924-A-G
• gnomAD v4: 4-186287770-A-G
• COSMIC: COSM4682183 ; COSM4682184
• MyVariant Identifiers: chr4:g.187208924A>G (hg19) ; chr4:g.186287770A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287770A>G , CM000666.2:g.186287770A>G	GRCh38
NC_000004.11:g.187208924A>G , CM000666.1:g.187208924A>G	GRCh37
NC_000004.10:g.187445918A>G	NCBI36
NG_008051.1:g.26807A>G , LRG_583:g.26807A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1663A>G (F11) MANE Select	ENSP00000384957.2:p.Thr555Ala
ENST00000264691.4:c.263A>G (F11)
ENST00000264692.8:c.1501A>G (F11)	ENSP00000264692.5:p.Thr501Ala
ENST00000403665.6:c.1663A>G (F11)	ENSP00000384957.2:p.Thr555Ala
ENST00000503841.1:n.182A>G (F11)
NM_000128.3:c.1663A>G , LRG_583t1:c.1663A>G (F11)	NP_000119.1:p.Thr555Ala
NR_033900.1:n.1066+658T>C (F11-AS1)
XM_005262821.2:c.1666A>G (F11)	XP_005262878.1:p.Thr556Ala
XM_005262822.2:c.1570A>G (F11)	XP_005262879.1:p.Thr524Ala
XM_005262823.2:c.1396A>G (F11)	XP_005262880.1:p.Thr466Ala
XM_006714137.1:c.1618A>G (F11)	XP_006714200.1:p.Thr540Ala
XM_005262821.4:c.1666A>G (F11)	XP_005262878.1:p.Thr556Ala
XM_005262822.4:c.1570A>G (F11)	XP_005262879.1:p.Thr524Ala
XM_005262823.4:c.1396A>G (F11)	XP_005262880.1:p.Thr466Ala
XM_006714137.3:c.1618A>G (F11)	XP_006714200.1:p.Thr540Ala
NM_000128.4:c.1663A>G (F11) MANE Select	NP_000119.1:p.Thr555Ala