Canonical Allele Identifier: CA1519938502

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285675_186285676delinsAT , CM000666.2:g.186285675_186285676delinsAT	GRCh38
NC_000004.11:g.187206829_187206830delinsAT , CM000666.1:g.187206829_187206830delinsAT	GRCh37
NC_000004.10:g.187443823_187443824delinsAT	NCBI36
NG_008051.1:g.24712_24713delinsAT , LRG_583:g.24712_24713delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1342_1343delinsAT MANE Select	ENSP00000384957.2:p.Ile448=
ENST00000264691.4:c.38_39delinsAT
ENST00000264692.8:c.1180_1181delinsAT	ENSP00000264692.5:p.Ile394=
ENST00000403665.6:c.1342_1343delinsAT	ENSP00000384957.2:p.Ile448=
NM_000128.3:c.1342_1343delinsAT , LRG_583t1:c.1342_1343delinsAT	NP_000119.1:p.Ile448=
XM_005262821.2:c.1345_1346delinsAT	XP_005262878.1:p.Ile449=
XM_005262822.2:c.1345_1346delinsAT	XP_005262879.1:p.Ile449=
XM_005262823.2:c.1075_1076delinsAT	XP_005262880.1:p.Ile359=
XM_005262824.1:c.1345_1346delinsAT	XP_005262881.1:p.Ile449=
XM_006714137.1:c.1297_1298delinsAT	XP_006714200.1:p.Ile433=
XR_938706.1:n.1750_1751delinsAT
XR_938707.1:n.1750_1751delinsAT
XM_005262821.4:c.1345_1346delinsAT	XP_005262878.1:p.Ile449=
XM_005262822.4:c.1345_1346delinsAT	XP_005262879.1:p.Ile449=
XM_005262823.4:c.1075_1076delinsAT	XP_005262880.1:p.Ile359=
XM_006714137.3:c.1297_1298delinsAT	XP_006714200.1:p.Ile433=
XR_001741172.2:n.1816_1817delinsAT
NM_000128.4:c.1342_1343delinsAT MANE Select	NP_000119.1:p.Ile448=