Canonical Allele Identifier: CA112102769

Gene: F11

Linked Data

• dbSNP Id: rs1554083590
• MyVariant Identifiers: chr4:g.187205777_187205778insG (hg19) ; chr4:g.186284623_186284624insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284623_186284624insG , CM000666.2:g.186284623_186284624insG	GRCh38
NC_000004.11:g.187205777_187205778insG , CM000666.1:g.187205777_187205778insG	GRCh37
NC_000004.10:g.187442771_187442772insG	NCBI36
NG_008051.1:g.23660_23661insG , LRG_583:g.23660_23661insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+363_1304+364insG MANE Select	ENSP00000384957.2:n.1304+363_1304+364insG
ENST00000264692.8:c.1142+363_1142+364insG	ENSP00000264692.5:n.1142+363_1142+364insG
ENST00000403665.6:c.1304+363_1304+364insG	ENSP00000384957.2:n.1304+363_1304+364insG
NM_000128.3:c.1304+363_1304+364insG , LRG_583t1:c.1304+363_1304+364insG	NP_000119.1:n.1304+363_1304+364insG
XM_005262821.2:c.1307+363_1307+364insG	XP_005262878.1:n.1307+363_1307+364insG
XM_005262822.2:c.1307+363_1307+364insG	XP_005262879.1:n.1307+363_1307+364insG
XM_005262823.2:c.1037+363_1037+364insG	XP_005262880.1:n.1037+363_1037+364insG
XM_005262824.1:c.1307+363_1307+364insG	XP_005262881.1:n.1307+363_1307+364insG
XM_006714137.1:c.1259+363_1259+364insG	XP_006714200.1:n.1259+363_1259+364insG
XR_938706.1:n.1712+363_1712+364insG
XR_938707.1:n.1712+363_1712+364insG
XM_005262821.4:c.1307+363_1307+364insG	XP_005262878.1:n.1307+363_1307+364insG
XM_005262822.4:c.1307+363_1307+364insG	XP_005262879.1:n.1307+363_1307+364insG
XM_005262823.4:c.1037+363_1037+364insG	XP_005262880.1:n.1037+363_1037+364insG
XM_006714137.3:c.1259+363_1259+364insG	XP_006714200.1:n.1259+363_1259+364insG
XR_001741172.2:n.1778+363_1778+364insG
NM_000128.4:c.1304+363_1304+364insG MANE Select	NP_000119.1:n.1304+363_1304+364insG