Canonical Allele Identifier: CA1519938514

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285707_186285711delinsATCTT , CM000666.2:g.186285707_186285711delinsATCTT	GRCh38
NC_000004.11:g.187206861_187206865delinsATCTT , CM000666.1:g.187206861_187206865delinsATCTT	GRCh37
NC_000004.10:g.187443855_187443859delinsATCTT	NCBI36
NG_008051.1:g.24744_24748delinsATCTT , LRG_583:g.24744_24748delinsATCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1374_1378delinsATCTT MANE Select	ENSP00000384957.2:p.Thr458=
ENST00000264691.4:c.70_74delinsATCTT
ENST00000264692.8:c.1212_1216delinsATCTT	ENSP00000264692.5:p.Thr404=
ENST00000403665.6:c.1374_1378delinsATCTT	ENSP00000384957.2:p.Thr458=
NM_000128.3:c.1374_1378delinsATCTT , LRG_583t1:c.1374_1378delinsATCTT	NP_000119.1:p.Thr458=
XM_005262821.2:c.1377_1381delinsATCTT	XP_005262878.1:p.Thr459=
XM_005262822.2:c.1377_1381delinsATCTT	XP_005262879.1:p.Thr459=
XM_005262823.2:c.1107_1111delinsATCTT	XP_005262880.1:p.Thr369=
XM_005262824.1:c.1377_1381delinsATCTT	XP_005262881.1:p.Thr459=
XM_006714137.1:c.1329_1333delinsATCTT	XP_006714200.1:p.Thr443=
XR_938706.1:n.1782_1786delinsATCTT
XR_938707.1:n.1782_1786delinsATCTT
XM_005262821.4:c.1377_1381delinsATCTT	XP_005262878.1:p.Thr459=
XM_005262822.4:c.1377_1381delinsATCTT	XP_005262879.1:p.Thr459=
XM_005262823.4:c.1107_1111delinsATCTT	XP_005262880.1:p.Thr369=
XM_006714137.3:c.1329_1333delinsATCTT	XP_006714200.1:p.Thr443=
XR_001741172.2:n.1848_1852delinsATCTT
NM_000128.4:c.1374_1378delinsATCTT MANE Select	NP_000119.1:p.Thr458=