Canonical Allele Identifier: CA1519937669

Gene: F11

Linked Data

• dbSNP Id: rs1740981568

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186283983del , CM000666.2:g.186283983del	GRCh38
NC_000004.11:g.187205137del , CM000666.1:g.187205137del	GRCh37
NC_000004.10:g.187442131del	NCBI36
NG_008051.1:g.23020del , LRG_583:g.23020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1136-109del MANE Select	ENSP00000384957.2:n.1136-109del
ENST00000264692.8:c.974-109del	ENSP00000264692.5:n.974-109del
ENST00000403665.6:c.1136-109del	ENSP00000384957.2:n.1136-109del
NM_000128.3:c.1136-109del , LRG_583t1:c.1136-109del	NP_000119.1:n.1136-109del
XM_005262821.2:c.1139-109del	XP_005262878.1:n.1139-109del
XM_005262822.2:c.1139-109del	XP_005262879.1:n.1139-109del
XM_005262823.2:c.869-109del	XP_005262880.1:n.869-109del
XM_005262824.1:c.1139-109del	XP_005262881.1:n.1139-109del
XM_006714137.1:c.1091-109del	XP_006714200.1:n.1091-109del
XR_938706.1:n.1544-109del
XR_938707.1:n.1544-109del
XM_005262821.4:c.1139-109del	XP_005262878.1:n.1139-109del
XM_005262822.4:c.1139-109del	XP_005262879.1:n.1139-109del
XM_005262823.4:c.869-109del	XP_005262880.1:n.869-109del
XM_006714137.3:c.1091-109del	XP_006714200.1:n.1091-109del
XM_017007884.2:c.*1999del	XP_016863373.1:n.*1999del
XM_017007885.2:c.*4-109del	XP_016863374.1:n.*4-109del
XR_001741172.2:n.1610-109del
NM_000128.4:c.1136-109del MANE Select	NP_000119.1:n.1136-109del