Canonical Allele Identifier: CA1519938655

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186286017_186286018delinsAG , CM000666.2:g.186286017_186286018delinsAG	GRCh38
NC_000004.11:g.187207171_187207172delinsAG , CM000666.1:g.187207171_187207172delinsAG	GRCh37
NC_000004.10:g.187444165_187444166delinsAG	NCBI36
NG_008051.1:g.25054_25055delinsAG , LRG_583:g.25054_25055delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1480+204_1480+205delinsAG MANE Select	ENSP00000384957.2:n.1480+204_1480+205delinsAG
ENST00000264691.4:c.176+204_176+205delinsAG
ENST00000264692.8:c.1318+204_1318+205delinsAG	ENSP00000264692.5:n.1318+204_1318+205delinsAG
ENST00000403665.6:c.1480+204_1480+205delinsAG	ENSP00000384957.2:n.1480+204_1480+205delinsAG
NM_000128.3:c.1480+204_1480+205delinsAG , LRG_583t1:c.1480+204_1480+205delinsAG	NP_000119.1:n.1480+204_1480+205delinsAG
XM_005262821.2:c.1483+204_1483+205delinsAG	XP_005262878.1:n.1483+204_1483+205delinsAG
XM_005262822.2:c.1483+204_1483+205delinsAG	XP_005262879.1:n.1483+204_1483+205delinsAG
XM_005262823.2:c.1213+204_1213+205delinsAG	XP_005262880.1:n.1213+204_1213+205delinsAG
XM_005262824.1:c.1483+204_1483+205delinsAG	XP_005262881.1:n.1483+204_1483+205delinsAG
XM_006714137.1:c.1435+204_1435+205delinsAG	XP_006714200.1:n.1435+204_1435+205delinsAG
XR_938706.1:n.1888+204_1888+205delinsAG
XR_938707.1:n.1888+204_1888+205delinsAG
XM_005262821.4:c.1483+204_1483+205delinsAG	XP_005262878.1:n.1483+204_1483+205delinsAG
XM_005262822.4:c.1483+204_1483+205delinsAG	XP_005262879.1:n.1483+204_1483+205delinsAG
XM_005262823.4:c.1213+204_1213+205delinsAG	XP_005262880.1:n.1213+204_1213+205delinsAG
XM_006714137.3:c.1435+204_1435+205delinsAG	XP_006714200.1:n.1435+204_1435+205delinsAG
XR_001741172.2:n.1954+204_1954+205delinsAG
NM_000128.4:c.1480+204_1480+205delinsAG MANE Select	NP_000119.1:n.1480+204_1480+205delinsAG