Canonical Allele Identifier: CA358944067

Gene: F11 F11-AS1

Linked Data

• gnomAD v4: 4-186286451-A-C
• MyVariant Identifiers: chr4:g.187207605A>C (hg19) ; chr4:g.186286451A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286451A>C , CM000666.2:g.186286451A>C	GRCh38
NC_000004.11:g.187207605A>C , CM000666.1:g.187207605A>C	GRCh37
NC_000004.10:g.187444599A>C	NCBI36
NG_008051.1:g.25488A>C , LRG_583:g.25488A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1517A>C (F11) MANE Select	ENSP00000384957.2:p.Asp506Ala
ENST00000264691.4:c.176+638A>C (F11)
ENST00000264692.8:c.1355A>C (F11)	ENSP00000264692.5:p.Asp452Ala
ENST00000403665.6:c.1517A>C (F11)	ENSP00000384957.2:p.Asp506Ala
NM_000128.3:c.1517A>C , LRG_583t1:c.1517A>C (F11)	NP_000119.1:p.Asp506Ala
NR_033900.1:n.1067-185T>G (F11-AS1)
XM_005262821.2:c.1520A>C (F11)	XP_005262878.1:p.Asp507Ala
XM_005262822.2:c.1483+638A>C (F11)	XP_005262879.1:n.1483+638A>C
XM_005262823.2:c.1250A>C (F11)	XP_005262880.1:p.Asp417Ala
XM_005262824.1:c.1484-95A>C (F11)	XP_005262881.1:n.1484-95A>C
XM_006714137.1:c.1472A>C (F11)	XP_006714200.1:p.Asp491Ala
XR_938706.1:n.1925A>C (F11)
XR_938707.1:n.1888+638A>C (F11)
XM_005262821.4:c.1520A>C (F11)	XP_005262878.1:p.Asp507Ala
XM_005262822.4:c.1483+638A>C (F11)	XP_005262879.1:n.1483+638A>C
XM_005262823.4:c.1250A>C (F11)	XP_005262880.1:p.Asp417Ala
XM_006714137.3:c.1472A>C (F11)	XP_006714200.1:p.Asp491Ala
XR_001741172.2:n.1991A>C (F11)
NM_000128.4:c.1517A>C (F11) MANE Select	NP_000119.1:p.Asp506Ala