Canonical Allele Identifier: CA1519938659

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286023_186286024delinsAC , CM000666.2:g.186286023_186286024delinsAC	GRCh38
NC_000004.11:g.187207177_187207178delinsAC , CM000666.1:g.187207177_187207178delinsAC	GRCh37
NC_000004.10:g.187444171_187444172delinsAC	NCBI36
NG_008051.1:g.25060_25061delinsAC , LRG_583:g.25060_25061delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1480+210_1480+211delinsAC MANE Select	ENSP00000384957.2:n.1480+210_1480+211delinsAC
ENST00000264691.4:c.176+210_176+211delinsAC
ENST00000264692.8:c.1318+210_1318+211delinsAC	ENSP00000264692.5:n.1318+210_1318+211delinsAC
ENST00000403665.6:c.1480+210_1480+211delinsAC	ENSP00000384957.2:n.1480+210_1480+211delinsAC
NM_000128.3:c.1480+210_1480+211delinsAC , LRG_583t1:c.1480+210_1480+211delinsAC	NP_000119.1:n.1480+210_1480+211delinsAC
XM_005262821.2:c.1483+210_1483+211delinsAC	XP_005262878.1:n.1483+210_1483+211delinsAC
XM_005262822.2:c.1483+210_1483+211delinsAC	XP_005262879.1:n.1483+210_1483+211delinsAC
XM_005262823.2:c.1213+210_1213+211delinsAC	XP_005262880.1:n.1213+210_1213+211delinsAC
XM_005262824.1:c.1483+210_1483+211delinsAC	XP_005262881.1:n.1483+210_1483+211delinsAC
XM_006714137.1:c.1435+210_1435+211delinsAC	XP_006714200.1:n.1435+210_1435+211delinsAC
XR_938706.1:n.1888+210_1888+211delinsAC
XR_938707.1:n.1888+210_1888+211delinsAC
XM_005262821.4:c.1483+210_1483+211delinsAC	XP_005262878.1:n.1483+210_1483+211delinsAC
XM_005262822.4:c.1483+210_1483+211delinsAC	XP_005262879.1:n.1483+210_1483+211delinsAC
XM_005262823.4:c.1213+210_1213+211delinsAC	XP_005262880.1:n.1213+210_1213+211delinsAC
XM_006714137.3:c.1435+210_1435+211delinsAC	XP_006714200.1:n.1435+210_1435+211delinsAC
XR_001741172.2:n.1954+210_1954+211delinsAC
NM_000128.4:c.1480+210_1480+211delinsAC MANE Select	NP_000119.1:n.1480+210_1480+211delinsAC