Canonical Allele Identifier: CA442639064

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205345_187205346del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284194_186284195del , CM000666.2:g.186284194_186284195del	GRCh38
NC_000004.11:g.187205348_187205349del , CM000666.1:g.187205348_187205349del	GRCh37
NC_000004.10:g.187442342_187442343del	NCBI36
NG_008051.1:g.23231_23232del , LRG_583:g.23231_23232del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1238_1239del MANE Select	ENSP00000384957.2:p.Arg413ThrfsTer27
ENST00000264692.8:c.1076_1077del	ENSP00000264692.5:p.Arg359ThrfsTer27
ENST00000403665.6:c.1238_1239del	ENSP00000384957.2:p.Arg413ThrfsTer27
NM_000128.3:c.1238_1239del , LRG_583t1:c.1238_1239del	NP_000119.1:p.Arg413ThrfsTer27
XM_005262821.2:c.1241_1242del	XP_005262878.1:p.Arg414ThrfsTer27
XM_005262822.2:c.1241_1242del	XP_005262879.1:p.Arg414ThrfsTer27
XM_005262823.2:c.971_972del	XP_005262880.1:p.Arg324ThrfsTer27
XM_005262824.1:c.1241_1242del	XP_005262881.1:p.Arg414ThrfsTer27
XM_006714137.1:c.1193_1194del	XP_006714200.1:p.Arg398ThrfsTer27
XR_938706.1:n.1646_1647del
XR_938707.1:n.1646_1647del
XM_005262821.4:c.1241_1242del	XP_005262878.1:p.Arg414ThrfsTer27
XM_005262822.4:c.1241_1242del	XP_005262879.1:p.Arg414ThrfsTer27
XM_005262823.4:c.971_972del	XP_005262880.1:p.Arg324ThrfsTer27
XM_006714137.3:c.1193_1194del	XP_006714200.1:p.Arg398ThrfsTer27
XR_001741172.2:n.1712_1713del
NM_000128.4:c.1238_1239del MANE Select	NP_000119.1:p.Arg413ThrfsTer27