Canonical Allele Identifier: CA3163754

Gene: F11

Linked Data

• dbSNP Id: rs761543485
• ExAC: 4:187197493 GTTGC / G
• gnomAD v2: 4-187197493-GTTGC-G
• gnomAD v3: 4-186276339-GTTGC-G
• gnomAD v4: 4-186276339-GTTGC-G
• MyVariant Identifiers: chr4:g.187197494_187197497del (hg19) ; chr4:g.186276340_186276343del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276343_186276346del , CM000666.2:g.186276343_186276346del	GRCh38
NC_000004.11:g.187197497_187197500del , CM000666.1:g.187197497_187197500del	GRCh37
NC_000004.10:g.187434491_187434494del	NCBI36
NG_008051.1:g.15380_15383del , LRG_583:g.15380_15383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.708_711del MANE Select	ENSP00000384957.2:p.Leu237PhefsTer?
ENST00000264692.8:c.546_549del	ENSP00000264692.5:p.Leu183PhefsTer?
ENST00000403665.6:c.708_711del	ENSP00000384957.2:p.Leu237PhefsTer?
ENST00000452239.1:c.155_158del
NM_000128.3:c.708_711del , LRG_583t1:c.708_711del	NP_000119.1:p.Leu237PhefsTer?
XM_005262821.2:c.708_711del	XP_005262878.1:p.Leu237PhefsTer?
XM_005262822.2:c.708_711del	XP_005262879.1:p.Leu237PhefsTer?
XM_005262823.2:c.485+2068_485+2071del	XP_005262880.1:n.485+2068_485+2071del
XM_005262824.1:c.708_711del	XP_005262881.1:p.Leu237PhefsTer?
XM_006714137.1:c.708_711del	XP_006714200.1:p.Leu237PhefsTer?
XR_938706.1:n.1060_1063del
XR_938707.1:n.1060_1063del
XM_005262821.4:c.708_711del	XP_005262878.1:p.Leu237PhefsTer?
XM_005262822.4:c.708_711del	XP_005262879.1:p.Leu237PhefsTer?
XM_005262823.4:c.485+2068_485+2071del	XP_005262880.1:n.485+2068_485+2071del
XM_006714137.3:c.708_711del	XP_006714200.1:p.Leu237PhefsTer?
XM_017007884.2:c.708_711del	XP_016863373.1:p.Leu237PhefsTer?
XM_017007885.2:c.708_711del	XP_016863374.1:p.Leu237PhefsTer?
XM_017007886.2:c.708_711del	XP_016863375.1:p.Leu237PhefsTer?
XR_001741172.2:n.1041_1044del
NM_000128.4:c.708_711del MANE Select	NP_000119.1:p.Leu237PhefsTer?