Canonical Allele Identifier: CA2672903420

Gene: F11

Linked Data

• gnomAD v4: 4-186283959-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186283962del , CM000666.2:g.186283962del	GRCh38
NC_000004.11:g.187205116del , CM000666.1:g.187205116del	GRCh37
NC_000004.10:g.187442110del	NCBI36
NG_008051.1:g.22999del , LRG_583:g.22999del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1136-130del MANE Select	ENSP00000384957.2:n.1136-130del
ENST00000264692.8:c.974-130del	ENSP00000264692.5:n.974-130del
ENST00000403665.6:c.1136-130del	ENSP00000384957.2:n.1136-130del
NM_000128.3:c.1136-130del , LRG_583t1:c.1136-130del	NP_000119.1:n.1136-130del
XM_005262821.2:c.1139-130del	XP_005262878.1:n.1139-130del
XM_005262822.2:c.1139-130del	XP_005262879.1:n.1139-130del
XM_005262823.2:c.869-130del	XP_005262880.1:n.869-130del
XM_005262824.1:c.1139-130del	XP_005262881.1:n.1139-130del
XM_006714137.1:c.1091-130del	XP_006714200.1:n.1091-130del
XR_938706.1:n.1544-130del
XR_938707.1:n.1544-130del
XM_005262821.4:c.1139-130del	XP_005262878.1:n.1139-130del
XM_005262822.4:c.1139-130del	XP_005262879.1:n.1139-130del
XM_005262823.4:c.869-130del	XP_005262880.1:n.869-130del
XM_006714137.3:c.1091-130del	XP_006714200.1:n.1091-130del
XM_017007884.2:c.*1978del	XP_016863373.1:n.*1978del
XM_017007885.2:c.*4-130del	XP_016863374.1:n.*4-130del
XR_001741172.2:n.1610-130del
NM_000128.4:c.1136-130del MANE Select	NP_000119.1:n.1136-130del