Canonical Allele Identifier: CA3164018

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286452T>C , CM000666.2:g.186286452T>C	GRCh38
NC_000004.11:g.187207606T>C , CM000666.1:g.187207606T>C	GRCh37
NC_000004.10:g.187444600T>C	NCBI36
NG_008051.1:g.25489T>C , LRG_583:g.25489T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1518T>C (F11) MANE Select	ENSP00000384957.2:p.Asp506=
ENST00000264691.4:c.176+639T>C (F11)
ENST00000264692.8:c.1356T>C (F11)	ENSP00000264692.5:p.Asp452=
ENST00000403665.6:c.1518T>C (F11)	ENSP00000384957.2:p.Asp506=
NM_000128.3:c.1518T>C , LRG_583t1:c.1518T>C (F11)	NP_000119.1:p.Asp506=
NR_033900.1:n.1067-186A>G (F11-AS1)
XM_005262821.2:c.1521T>C (F11)	XP_005262878.1:p.Asp507=
XM_005262822.2:c.1483+639T>C (F11)	XP_005262879.1:n.1483+639T>C
XM_005262823.2:c.1251T>C (F11)	XP_005262880.1:p.Asp417=
XM_005262824.1:c.1484-94T>C (F11)	XP_005262881.1:n.1484-94T>C
XM_006714137.1:c.1473T>C (F11)	XP_006714200.1:p.Asp491=
XR_938706.1:n.1926T>C (F11)
XR_938707.1:n.1888+639T>C (F11)
XM_005262821.4:c.1521T>C (F11)	XP_005262878.1:p.Asp507=
XM_005262822.4:c.1483+639T>C (F11)	XP_005262879.1:n.1483+639T>C
XM_005262823.4:c.1251T>C (F11)	XP_005262880.1:p.Asp417=
XM_006714137.3:c.1473T>C (F11)	XP_006714200.1:p.Asp491=
XR_001741172.2:n.1992T>C (F11)
NM_000128.4:c.1518T>C (F11) MANE Select	NP_000119.1:p.Asp506=