Canonical Allele Identifier: CA557396084

Gene: F11

Linked Data

• dbSNP Id: rs1252620154
• gnomAD v2: 4-187201339-AGG-A
• MyVariant Identifiers: chr4:g.187201340_187201341del (hg19) ; chr4:g.186280186_186280187del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280187_186280188del , CM000666.2:g.186280187_186280188del	GRCh38
NC_000004.11:g.187201341_187201342del , CM000666.1:g.187201341_187201342del	GRCh37
NC_000004.10:g.187438335_187438336del	NCBI36
NG_008051.1:g.19224_19225del , LRG_583:g.19224_19225del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.866-36_866-35del MANE Select	ENSP00000384957.2:n.866-36_866-35del
ENST00000264692.8:c.704-36_704-35del	ENSP00000264692.5:n.704-36_704-35del
ENST00000403665.6:c.866-36_866-35del	ENSP00000384957.2:n.866-36_866-35del
ENST00000452239.1:c.313-36_313-35del
NM_000128.3:c.866-36_866-35del , LRG_583t1:c.866-36_866-35del	NP_000119.1:n.866-36_866-35del
XM_005262821.2:c.866-36_866-35del	XP_005262878.1:n.866-36_866-35del
XM_005262822.2:c.866-36_866-35del	XP_005262879.1:n.866-36_866-35del
XM_005262823.2:c.596-36_596-35del	XP_005262880.1:n.596-36_596-35del
XM_005262824.1:c.866-36_866-35del	XP_005262881.1:n.866-36_866-35del
XM_006714137.1:c.865+66_865+67del	XP_006714200.1:n.865+66_865+67del
XR_938706.1:n.1218-36_1218-35del
XR_938707.1:n.1218-36_1218-35del
XM_005262821.4:c.866-36_866-35del	XP_005262878.1:n.866-36_866-35del
XM_005262822.4:c.866-36_866-35del	XP_005262879.1:n.866-36_866-35del
XM_005262823.4:c.596-36_596-35del	XP_005262880.1:n.596-36_596-35del
XM_006714137.3:c.865+66_865+67del	XP_006714200.1:n.865+66_865+67del
XM_017007884.2:c.866-36_866-35del	XP_016863373.1:n.866-36_866-35del
XM_017007885.2:c.866-36_866-35del	XP_016863374.1:n.866-36_866-35del
XM_017007886.2:c.866-36_866-35del	XP_016863375.1:n.866-36_866-35del
XR_001741172.2:n.1199-36_1199-35del
NM_000128.4:c.866-36_866-35del MANE Select	NP_000119.1:n.866-36_866-35del