Canonical Allele Identifier: CA2831038896

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285654del , CM000666.2:g.186285654del	GRCh38
NC_000004.11:g.187206808del , CM000666.1:g.187206808del	GRCh37
NC_000004.10:g.187443802del	NCBI36
NG_008051.1:g.24691del , LRG_583:g.24691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1321del MANE Select	ENSP00000384957.2:p.Ile441PhefsTer9
ENST00000264691.4:c.17del
ENST00000264692.8:c.1159del	ENSP00000264692.5:p.Ile387PhefsTer9
ENST00000403665.6:c.1321del	ENSP00000384957.2:p.Ile441PhefsTer9
NM_000128.3:c.1321del , LRG_583t1:c.1321del	NP_000119.1:p.Ile441PhefsTer9
XM_005262821.2:c.1324del	XP_005262878.1:p.Ile442PhefsTer9
XM_005262822.2:c.1324del	XP_005262879.1:p.Ile442PhefsTer9
XM_005262823.2:c.1054del	XP_005262880.1:p.Ile352PhefsTer9
XM_005262824.1:c.1324del	XP_005262881.1:p.Ile442PhefsTer9
XM_006714137.1:c.1276del	XP_006714200.1:p.Ile426PhefsTer9
XR_938706.1:n.1729del
XR_938707.1:n.1729del
XM_005262821.4:c.1324del	XP_005262878.1:p.Ile442PhefsTer9
XM_005262822.4:c.1324del	XP_005262879.1:p.Ile442PhefsTer9
XM_005262823.4:c.1054del	XP_005262880.1:p.Ile352PhefsTer9
XM_006714137.3:c.1276del	XP_006714200.1:p.Ile426PhefsTer9
XR_001741172.2:n.1795del
NM_000128.4:c.1321del MANE Select	NP_000119.1:p.Ile441PhefsTer9