Canonical Allele Identifier: CA792316556

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1352524190
• MyVariant Identifiers: chr4:g.187208743_187208744insATAT (hg19) ; chr4:g.186287589_186287590insATAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287590_186287591insTATA , CM000666.2:g.186287590_186287591insTATA	GRCh38
NC_000004.11:g.187208744_187208745insTATA , CM000666.1:g.187208744_187208745insTATA	GRCh37
NC_000004.10:g.187445738_187445739insTATA	NCBI36
NG_008051.1:g.26627_26628insTATA , LRG_583:g.26627_26628insTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1577-94_1577-93insTATA (F11) MANE Select	ENSP00000384957.2:n.1577-94_1577-93insTATA
ENST00000264691.4:c.177-94_177-93insTATA (F11)
ENST00000264692.8:c.1415-94_1415-93insTATA (F11)	ENSP00000264692.5:n.1415-94_1415-93insTATA
ENST00000403665.6:c.1577-94_1577-93insTATA (F11)	ENSP00000384957.2:n.1577-94_1577-93insTATA
ENST00000503841.1:n.2_3insTATA (F11)
NM_000128.3:c.1577-94_1577-93insTATA , LRG_583t1:c.1577-94_1577-93insTATA (F11)	NP_000119.1:n.1577-94_1577-93insTATA
NR_033900.1:n.1066+838_1066+839insATAT (F11-AS1)
XM_005262821.2:c.1580-94_1580-93insTATA (F11)	XP_005262878.1:n.1580-94_1580-93insTATA
XM_005262822.2:c.1484-94_1484-93insTATA (F11)	XP_005262879.1:n.1484-94_1484-93insTATA
XM_005262823.2:c.1310-94_1310-93insTATA (F11)	XP_005262880.1:n.1310-94_1310-93insTATA
XM_006714137.1:c.1532-94_1532-93insTATA (F11)	XP_006714200.1:n.1532-94_1532-93insTATA
XR_938706.1:n.1985-94_1985-93insTATA (F11)
XR_938707.1:n.1889-94_1889-93insTATA (F11)
XM_005262821.4:c.1580-94_1580-93insTATA (F11)	XP_005262878.1:n.1580-94_1580-93insTATA
XM_005262822.4:c.1484-94_1484-93insTATA (F11)	XP_005262879.1:n.1484-94_1484-93insTATA
XM_005262823.4:c.1310-94_1310-93insTATA (F11)	XP_005262880.1:n.1310-94_1310-93insTATA
XM_006714137.3:c.1532-94_1532-93insTATA (F11)	XP_006714200.1:n.1532-94_1532-93insTATA
NM_000128.4:c.1577-94_1577-93insTATA (F11) MANE Select	NP_000119.1:n.1577-94_1577-93insTATA