Canonical Allele Identifier: CA112146622

Gene: F11

Linked Data

• dbSNP Id: rs1554081272
• MyVariant Identifiers: chr4:g.187188142_187188143insAT (hg19) ; chr4:g.186266988_186266989insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186266989_186266990insTA , CM000666.2:g.186266989_186266990insTA	GRCh38
NC_000004.11:g.187188143_187188144insTA , CM000666.1:g.187188143_187188144insTA	GRCh37
NC_000004.10:g.187425137_187425138insTA	NCBI36
NG_008051.1:g.6026_6027insTA , LRG_583:g.6026_6027insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.-1-147_-1-146insTA MANE Select	ENSP00000384957.2:n.-1-147_-1-146insTA
ENST00000264692.8:c.-1-147_-1-146insTA	ENSP00000264692.5:n.-1-147_-1-146insTA
ENST00000403665.6:c.-1-147_-1-146insTA	ENSP00000384957.2:n.-1-147_-1-146insTA
ENST00000492972.6:c.-1-147_-1-146insTA	ENSP00000424479.1:n.-1-147_-1-146insTA
NM_000128.3:c.-1-147_-1-146insTA , LRG_583t1:c.-1-147_-1-146insTA	NP_000119.1:n.-1-147_-1-146insTA
XM_005262821.2:c.-1-147_-1-146insTA	XP_005262878.1:n.-1-147_-1-146insTA
XM_005262822.2:c.-1-147_-1-146insTA	XP_005262879.1:n.-1-147_-1-146insTA
XM_005262823.2:c.-1-147_-1-146insTA	XP_005262880.1:n.-1-147_-1-146insTA
XM_005262824.1:c.-1-147_-1-146insTA	XP_005262881.1:n.-1-147_-1-146insTA
XM_006714137.1:c.-1-147_-1-146insTA	XP_006714200.1:n.-1-147_-1-146insTA
XR_938706.1:n.352-147_352-146insTA
XR_938707.1:n.352-147_352-146insTA
NM_001354804.1:c.-1-147_-1-146insTA	NP_001341733.1:n.-1-147_-1-146insTA
XM_005262821.4:c.-1-147_-1-146insTA	XP_005262878.1:n.-1-147_-1-146insTA
XM_005262822.4:c.-1-147_-1-146insTA	XP_005262879.1:n.-1-147_-1-146insTA
XM_005262823.4:c.-1-147_-1-146insTA	XP_005262880.1:n.-1-147_-1-146insTA
XM_006714137.3:c.-1-147_-1-146insTA	XP_006714200.1:n.-1-147_-1-146insTA
XM_017007884.2:c.-1-147_-1-146insTA	XP_016863373.1:n.-1-147_-1-146insTA
XM_017007885.2:c.-1-147_-1-146insTA	XP_016863374.1:n.-1-147_-1-146insTA
XM_017007886.2:c.-1-147_-1-146insTA	XP_016863375.1:n.-1-147_-1-146insTA
XR_001741172.2:n.333-147_333-146insTA
NM_000128.4:c.-1-147_-1-146insTA MANE Select	NP_000119.1:n.-1-147_-1-146insTA
NM_001354804.2:c.-1-147_-1-146insTA	NP_001341733.1:n.-1-147_-1-146insTA