Canonical Allele Identifier: CA1519938567

Gene: F11

Linked Data

• dbSNP Id: rs1741170969

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285839del , CM000666.2:g.186285839del	GRCh38
NC_000004.11:g.187206993del , CM000666.1:g.187206993del	GRCh37
NC_000004.10:g.187443987del	NCBI36
NG_008051.1:g.24876del , LRG_583:g.24876del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1480+26del MANE Select	ENSP00000384957.2:n.1480+26del
ENST00000264691.4:c.176+26del
ENST00000264692.8:c.1318+26del	ENSP00000264692.5:n.1318+26del
ENST00000403665.6:c.1480+26del	ENSP00000384957.2:n.1480+26del
NM_000128.3:c.1480+26del , LRG_583t1:c.1480+26del	NP_000119.1:n.1480+26del
XM_005262821.2:c.1483+26del	XP_005262878.1:n.1483+26del
XM_005262822.2:c.1483+26del	XP_005262879.1:n.1483+26del
XM_005262823.2:c.1213+26del	XP_005262880.1:n.1213+26del
XM_005262824.1:c.1483+26del	XP_005262881.1:n.1483+26del
XM_006714137.1:c.1435+26del	XP_006714200.1:n.1435+26del
XR_938706.1:n.1888+26del
XR_938707.1:n.1888+26del
XM_005262821.4:c.1483+26del	XP_005262878.1:n.1483+26del
XM_005262822.4:c.1483+26del	XP_005262879.1:n.1483+26del
XM_005262823.4:c.1213+26del	XP_005262880.1:n.1213+26del
XM_006714137.3:c.1435+26del	XP_006714200.1:n.1435+26del
XR_001741172.2:n.1954+26del
NM_000128.4:c.1480+26del MANE Select	NP_000119.1:n.1480+26del