Canonical Allele Identifier: CA1519938566

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285837_186285838delinsGT , CM000666.2:g.186285837_186285838delinsGT	GRCh38
NC_000004.11:g.187206991_187206992delinsGT , CM000666.1:g.187206991_187206992delinsGT	GRCh37
NC_000004.10:g.187443985_187443986delinsGT	NCBI36
NG_008051.1:g.24874_24875delinsGT , LRG_583:g.24874_24875delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1480+24_1480+25delinsGT MANE Select	ENSP00000384957.2:n.1480+24_1480+25delinsGT
ENST00000264691.4:c.176+24_176+25delinsGT
ENST00000264692.8:c.1318+24_1318+25delinsGT	ENSP00000264692.5:n.1318+24_1318+25delinsGT
ENST00000403665.6:c.1480+24_1480+25delinsGT	ENSP00000384957.2:n.1480+24_1480+25delinsGT
NM_000128.3:c.1480+24_1480+25delinsGT , LRG_583t1:c.1480+24_1480+25delinsGT	NP_000119.1:n.1480+24_1480+25delinsGT
XM_005262821.2:c.1483+24_1483+25delinsGT	XP_005262878.1:n.1483+24_1483+25delinsGT
XM_005262822.2:c.1483+24_1483+25delinsGT	XP_005262879.1:n.1483+24_1483+25delinsGT
XM_005262823.2:c.1213+24_1213+25delinsGT	XP_005262880.1:n.1213+24_1213+25delinsGT
XM_005262824.1:c.1483+24_1483+25delinsGT	XP_005262881.1:n.1483+24_1483+25delinsGT
XM_006714137.1:c.1435+24_1435+25delinsGT	XP_006714200.1:n.1435+24_1435+25delinsGT
XR_938706.1:n.1888+24_1888+25delinsGT
XR_938707.1:n.1888+24_1888+25delinsGT
XM_005262821.4:c.1483+24_1483+25delinsGT	XP_005262878.1:n.1483+24_1483+25delinsGT
XM_005262822.4:c.1483+24_1483+25delinsGT	XP_005262879.1:n.1483+24_1483+25delinsGT
XM_005262823.4:c.1213+24_1213+25delinsGT	XP_005262880.1:n.1213+24_1213+25delinsGT
XM_006714137.3:c.1435+24_1435+25delinsGT	XP_006714200.1:n.1435+24_1435+25delinsGT
XR_001741172.2:n.1954+24_1954+25delinsGT
NM_000128.4:c.1480+24_1480+25delinsGT MANE Select	NP_000119.1:n.1480+24_1480+25delinsGT