Canonical Allele Identifier: CA112146615

Gene: F11

Linked Data

• ClinVar Variation Id: 1294834
• ClinVar RCV Id: RCV001720738
• dbSNP Id: rs3841991
• gnomAD v2: 4-187188141-G-GAT
• gnomAD v3: 4-186266987-G-GAT
• gnomAD v4: 4-186266987-G-GAT
• MyVariant Identifiers: chr4:g.187188142_187188143insTA (hg19) ; chr4:g.187188141_187188142insAT (hg19) ; chr4:g.186266988_186266989insTA (hg38) ; chr4:g.186266987_186266988insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186266988_186266989insTA , CM000666.2:g.186266988_186266989insTA	GRCh38
NC_000004.11:g.187188142_187188143insTA , CM000666.1:g.187188142_187188143insTA	GRCh37
NC_000004.10:g.187425136_187425137insTA	NCBI36
NG_008051.1:g.6025_6026insTA , LRG_583:g.6025_6026insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.-1-148_-1-147insTA MANE Select	ENSP00000384957.2:n.-1-148_-1-147insTA
ENST00000264692.8:c.-1-148_-1-147insTA	ENSP00000264692.5:n.-1-148_-1-147insTA
ENST00000403665.6:c.-1-148_-1-147insTA	ENSP00000384957.2:n.-1-148_-1-147insTA
ENST00000492972.6:c.-1-148_-1-147insTA	ENSP00000424479.1:n.-1-148_-1-147insTA
NM_000128.3:c.-1-148_-1-147insTA , LRG_583t1:c.-1-148_-1-147insTA	NP_000119.1:n.-1-148_-1-147insTA
XM_005262821.2:c.-1-148_-1-147insTA	XP_005262878.1:n.-1-148_-1-147insTA
XM_005262822.2:c.-1-148_-1-147insTA	XP_005262879.1:n.-1-148_-1-147insTA
XM_005262823.2:c.-1-148_-1-147insTA	XP_005262880.1:n.-1-148_-1-147insTA
XM_005262824.1:c.-1-148_-1-147insTA	XP_005262881.1:n.-1-148_-1-147insTA
XM_006714137.1:c.-1-148_-1-147insTA	XP_006714200.1:n.-1-148_-1-147insTA
XR_938706.1:n.352-148_352-147insTA
XR_938707.1:n.352-148_352-147insTA
NM_001354804.1:c.-1-148_-1-147insTA	NP_001341733.1:n.-1-148_-1-147insTA
XM_005262821.4:c.-1-148_-1-147insTA	XP_005262878.1:n.-1-148_-1-147insTA
XM_005262822.4:c.-1-148_-1-147insTA	XP_005262879.1:n.-1-148_-1-147insTA
XM_005262823.4:c.-1-148_-1-147insTA	XP_005262880.1:n.-1-148_-1-147insTA
XM_006714137.3:c.-1-148_-1-147insTA	XP_006714200.1:n.-1-148_-1-147insTA
XM_017007884.2:c.-1-148_-1-147insTA	XP_016863373.1:n.-1-148_-1-147insTA
XM_017007885.2:c.-1-148_-1-147insTA	XP_016863374.1:n.-1-148_-1-147insTA
XM_017007886.2:c.-1-148_-1-147insTA	XP_016863375.1:n.-1-148_-1-147insTA
XR_001741172.2:n.333-148_333-147insTA
NM_000128.4:c.-1-148_-1-147insTA MANE Select	NP_000119.1:n.-1-148_-1-147insTA
NM_001354804.2:c.-1-148_-1-147insTA	NP_001341733.1:n.-1-148_-1-147insTA