Canonical Allele Identifier: CA557396069

Gene: F11

Linked Data

• dbSNP Id: rs1561486348
• gnomAD v2: 4-187201226-CA-C
• MyVariant Identifiers: chr4:g.187201227del (hg19) ; chr4:g.186280073del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280075del , CM000666.2:g.186280075del	GRCh38
NC_000004.11:g.187201229del , CM000666.1:g.187201229del	GRCh37
NC_000004.10:g.187438223del	NCBI36
NG_008051.1:g.19112del , LRG_583:g.19112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.819del MANE Select	ENSP00000384957.2:p.Ala274LeufsTer?
ENST00000264692.8:c.657del	ENSP00000264692.5:p.Ala220LeufsTer?
ENST00000403665.6:c.819del	ENSP00000384957.2:p.Ala274LeufsTer?
ENST00000452239.1:c.266del
NM_000128.3:c.819del , LRG_583t1:c.819del	NP_000119.1:p.Ala274LeufsTer?
XM_005262821.2:c.819del	XP_005262878.1:p.Ala274LeufsTer?
XM_005262822.2:c.819del	XP_005262879.1:p.Ala274LeufsTer?
XM_005262823.2:c.549del	XP_005262880.1:p.Ala184LeufsTer?
XM_005262824.1:c.819del	XP_005262881.1:p.Ala274LeufsTer?
XM_006714137.1:c.819del	XP_006714200.1:p.Ala274LeufsTer?
XR_938706.1:n.1171del
XR_938707.1:n.1171del
XM_005262821.4:c.819del	XP_005262878.1:p.Ala274LeufsTer?
XM_005262822.4:c.819del	XP_005262879.1:p.Ala274LeufsTer?
XM_005262823.4:c.549del	XP_005262880.1:p.Ala184LeufsTer?
XM_006714137.3:c.819del	XP_006714200.1:p.Ala274LeufsTer?
XM_017007884.2:c.819del	XP_016863373.1:p.Ala274LeufsTer?
XM_017007885.2:c.819del	XP_016863374.1:p.Ala274LeufsTer?
XM_017007886.2:c.819del	XP_016863375.1:p.Ala274LeufsTer?
XR_001741172.2:n.1152del
NM_000128.4:c.819del MANE Select	NP_000119.1:p.Ala274LeufsTer?