Canonical Allele Identifier: CA358938907

Gene: F11

Linked Data

• dbSNP Id: rs1188870700
• gnomAD v2: 4-187201696-T-A
• gnomAD v4: 4-186280542-T-A
• MyVariant Identifiers: chr4:g.187201696T>A (hg19) ; chr4:g.186280542T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280542T>A , CM000666.2:g.186280542T>A	GRCh38
NC_000004.11:g.187201696T>A , CM000666.1:g.187201696T>A	GRCh37
NC_000004.10:g.187438690T>A	NCBI36
NG_008051.1:g.19579T>A , LRG_583:g.19579T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1097T>A MANE Select	ENSP00000384957.2:p.Ile366Asn
ENST00000264692.8:c.935T>A	ENSP00000264692.5:p.Ile312Asn
ENST00000403665.6:c.1097T>A	ENSP00000384957.2:p.Ile366Asn
ENST00000452239.1:c.544T>A
NM_000128.3:c.1097T>A , LRG_583t1:c.1097T>A	NP_000119.1:p.Ile366Asn
XM_005262821.2:c.1100T>A	XP_005262878.1:p.Ile367Asn
XM_005262822.2:c.1100T>A	XP_005262879.1:p.Ile367Asn
XM_005262823.2:c.830T>A	XP_005262880.1:p.Ile277Asn
XM_005262824.1:c.1100T>A	XP_005262881.1:p.Ile367Asn
XM_006714137.1:c.1052T>A	XP_006714200.1:p.Ile351Asn
XR_938706.1:n.1452T>A
XR_938707.1:n.1452T>A
XM_005262821.4:c.1100T>A	XP_005262878.1:p.Ile367Asn
XM_005262822.4:c.1100T>A	XP_005262879.1:p.Ile367Asn
XM_005262823.4:c.830T>A	XP_005262880.1:p.Ile277Asn
XM_006714137.3:c.1052T>A	XP_006714200.1:p.Ile351Asn
XM_017007884.2:c.1100T>A	XP_016863373.1:p.Ile367Asn
XM_017007885.2:c.1100T>A	XP_016863374.1:p.Ile367Asn
XM_017007886.2:c.1097T>A	XP_016863375.1:p.Ile366Asn
XR_001741172.2:n.1518T>A
NM_000128.4:c.1097T>A MANE Select	NP_000119.1:p.Ile366Asn