Canonical Allele Identifier: CA3163770

Gene: F11

Linked Data

• dbSNP Id: rs531180622
• ExAC: 4:187201126 TTGATA / T
• gnomAD v2: 4-187201126-TTGATA-T
• gnomAD v3: 4-186279972-TTGATA-T
• gnomAD v4: 4-186279972-TTGATA-T
• MyVariant Identifiers: chr4:g.187201127_187201131del (hg19) ; chr4:g.186279973_186279977del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186279979_186279983del , CM000666.2:g.186279979_186279983del	GRCh38
NC_000004.11:g.187201133_187201137del , CM000666.1:g.187201133_187201137del	GRCh37
NC_000004.10:g.187438127_187438131del	NCBI36
NG_008051.1:g.19016_19020del , LRG_583:g.19016_19020del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.756-33_756-29del MANE Select	ENSP00000384957.2:n.756-33_756-29del
ENST00000264692.8:c.594-33_594-29del	ENSP00000264692.5:n.594-33_594-29del
ENST00000403665.6:c.756-33_756-29del	ENSP00000384957.2:n.756-33_756-29del
ENST00000452239.1:c.203-33_203-29del
NM_000128.3:c.756-33_756-29del , LRG_583t1:c.756-33_756-29del	NP_000119.1:n.756-33_756-29del
XM_005262821.2:c.756-33_756-29del	XP_005262878.1:n.756-33_756-29del
XM_005262822.2:c.756-33_756-29del	XP_005262879.1:n.756-33_756-29del
XM_005262823.2:c.486-33_486-29del	XP_005262880.1:n.486-33_486-29del
XM_005262824.1:c.756-33_756-29del	XP_005262881.1:n.756-33_756-29del
XM_006714137.1:c.756-33_756-29del	XP_006714200.1:n.756-33_756-29del
XR_938706.1:n.1108-33_1108-29del
XR_938707.1:n.1108-33_1108-29del
XM_005262821.4:c.756-33_756-29del	XP_005262878.1:n.756-33_756-29del
XM_005262822.4:c.756-33_756-29del	XP_005262879.1:n.756-33_756-29del
XM_005262823.4:c.486-33_486-29del	XP_005262880.1:n.486-33_486-29del
XM_006714137.3:c.756-33_756-29del	XP_006714200.1:n.756-33_756-29del
XM_017007884.2:c.756-33_756-29del	XP_016863373.1:n.756-33_756-29del
XM_017007885.2:c.756-33_756-29del	XP_016863374.1:n.756-33_756-29del
XM_017007886.2:c.756-33_756-29del	XP_016863375.1:n.756-33_756-29del
XR_001741172.2:n.1089-33_1089-29del
NM_000128.4:c.756-33_756-29del MANE Select	NP_000119.1:n.756-33_756-29del