Canonical Allele Identifier: CA1519938583

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285866_186285867delinsGT , CM000666.2:g.186285866_186285867delinsGT	GRCh38
NC_000004.11:g.187207020_187207021delinsGT , CM000666.1:g.187207020_187207021delinsGT	GRCh37
NC_000004.10:g.187444014_187444015delinsGT	NCBI36
NG_008051.1:g.24903_24904delinsGT , LRG_583:g.24903_24904delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1480+53_1480+54delinsGT MANE Select	ENSP00000384957.2:n.1480+53_1480+54delinsGT
ENST00000264691.4:c.176+53_176+54delinsGT
ENST00000264692.8:c.1318+53_1318+54delinsGT	ENSP00000264692.5:n.1318+53_1318+54delinsGT
ENST00000403665.6:c.1480+53_1480+54delinsGT	ENSP00000384957.2:n.1480+53_1480+54delinsGT
NM_000128.3:c.1480+53_1480+54delinsGT , LRG_583t1:c.1480+53_1480+54delinsGT	NP_000119.1:n.1480+53_1480+54delinsGT
XM_005262821.2:c.1483+53_1483+54delinsGT	XP_005262878.1:n.1483+53_1483+54delinsGT
XM_005262822.2:c.1483+53_1483+54delinsGT	XP_005262879.1:n.1483+53_1483+54delinsGT
XM_005262823.2:c.1213+53_1213+54delinsGT	XP_005262880.1:n.1213+53_1213+54delinsGT
XM_005262824.1:c.1483+53_1483+54delinsGT	XP_005262881.1:n.1483+53_1483+54delinsGT
XM_006714137.1:c.1435+53_1435+54delinsGT	XP_006714200.1:n.1435+53_1435+54delinsGT
XR_938706.1:n.1888+53_1888+54delinsGT
XR_938707.1:n.1888+53_1888+54delinsGT
XM_005262821.4:c.1483+53_1483+54delinsGT	XP_005262878.1:n.1483+53_1483+54delinsGT
XM_005262822.4:c.1483+53_1483+54delinsGT	XP_005262879.1:n.1483+53_1483+54delinsGT
XM_005262823.4:c.1213+53_1213+54delinsGT	XP_005262880.1:n.1213+53_1213+54delinsGT
XM_006714137.3:c.1435+53_1435+54delinsGT	XP_006714200.1:n.1435+53_1435+54delinsGT
XR_001741172.2:n.1954+53_1954+54delinsGT
NM_000128.4:c.1480+53_1480+54delinsGT MANE Select	NP_000119.1:n.1480+53_1480+54delinsGT